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Areas Training Seminars and Classes
From Jack Quinn Solutions, L. L.C
CPSM Certification Coaching Online Course - ...ch to the study materials A clear understanding of what areas need immediate attention Specific plan to achieve success The confidence required to be successful Content The CPSM Certification Coaching consists of the study strategies, videos and audio files from the intense 3-day course where supply leaders are prepared to successfullya PASS the CPSM / CSM Exams  more...
From Certified Foreclosure Agent Program
Market Econometrics 210 - Coldwell Banker It's critical that agents understand how the local, regional and national economies affect the commercial real estate foreclosure market in their areas.  more...
From Healing Art Forms Institute
Holistic Healing Minute with Nicole Lanning Have you attempted to heal yourself or others through healing? Are you seeking a way to create a lifestyle that you are in control of? What about further developing your spiritual pathway with enlightenment and advanced awareness? Holistic Healing Minute offers all of this and so much more! Nicole Lanning, psychic intuitive, healer, and author, is now at your fingertips with a mind-blowing  more...
From Requirements Solutions Group
How to Plan Business Analysis Activities and Manage Risks instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewarecase study, exercises ...oject failure, paying special attention to these critical areas would seem to be a good idea. This virtual workshop focuses on the first half of techniques recommended by the International Institute of Business Analysis (IIBA ® in the Business Analysis Body of Knowledge (BABOK ®). Targeting senior business analysts, we present and apply techniques that plan how requiremetns will be  more...
How to Manage Changing Requirements instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewarecase study, exercises Managing requirements change has been a major challenge even for the best-run projects. Keeping track of how the changing business environment impacts ongoing projects and production applications can be a nightmare without proper tools and techniques. The concept of requirements management is not new but with an increase in the use of off-shore developers and off-the-shelf solutions, it has become  more...
How to Package and Communicate Business Requirements instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewarecase study, exercises One of the primary jobs of the business analyst is bridging the communication gap between the business community and the technology experts. Business, stakeholder, solution, and transition requirements describe what information technology has to deliver but making sure that both parties agree on just what these requirements mean is the real challenge. This virtual workshop presents concepts,  more...
From Data-Scribe (r)
CiviCRM Next Level Training instructor led trainingon-line e-learning cbt (computer based) Once you've attended our Getting Started with CiviCRM introductory workshop, you might want more in depth training on specific areas of CiviCRM. Our additional training levels would be a great follow-up for you. Training can be held privately for individuals or groups. You also can attend an upcoming public session, which is held in a Webinar format.  more...
From TypeLabs
TypeLabs presents 8 Keys to Self-Leadership with Dario Nardi instructor led trainingon-line e-learning cbt (computer based) ...rganizations. Specifically, we look at eight key strength areas, skill-building activiates to gain proficiency in those areas, and coaching questions to move people and teams. Participants receive a 5-page handout to review beforehand. This program is aimed at trainers, coaches, and managers, and uses the Jungian model of 8 cognitive processes. Participants will learn specific clues to look  more...
From PMSoft Consultancy Pvt. Ltd
Accelerated PMP E Learning instructor led trainingon-line e-learning cbt (computer based) Introduction: This training program is conducted to expose the participants to an integrated approach to Project Management. It is designed to develop the necessary knowledge needed to manage projects effectively. Key Features: Live Online sessions, 7 lectures of 3 hrs each only on weekends, to continue for 4 weeks. Opportunity to discuss directly with the faculty & clarify all  more...
From Webucator
MOC 5047 - Introduction to Installing and Managing Microsoft Exchange Server 2007 SP1 In this Microsoft Exchange training class, students who are new to Microsoft Exchange Server will learn how to configure and manage a messaging environment in accordance with technical requirements. Students will learn how to install Microsoft Exchange Server 2007 and manage routing, client access, and the backup and restore of databases. They will also learn how to manage addressing and recipient  more...
Introduction to Captivate 4 Training instructor led training This Captivate training class will introduce you to the essential Adobe Captivate 4 skills you need to know to get up and running with Captivate as quickly as possible. Using Adobe Captivate 4, you can capture screen shots on your computer and quickly turn them into lessons or movies. The movies you create can be interactive and you can add images, captions, rollovers, clickable areas, typing  more...
Groovy Training for Java Developers instructor led training ...nstructor, consultant, and developer specializing in all areas of Java, XML, and, more recently, Groovy and Grails. Over the past decade, he has taught courses and made presentations on topics ranging from Spring to Hibernate to Ajax to web services. His credentials include many industry certifications as well as several academic degrees, including two bachelors degrees from MIT two master  more...
Web Development using Grails instructor led training ...nstructor, consultant, and developer specializing in all areas of Java, XML, and, more recently, Groovy and Grails. Over the past decade, he has taught courses and made presentations on topics ranging from Spring to Hibernate to Ajax to web services. His credentials include many industry certifications as well as several academic degrees, including two bachelors degrees from MIT two master  more...
MOC 6420 - Fundamentals of Windows Server 2008 Network and Applications Infrastructure This Windows Server 2008 training class introduces students to network and applications infrastructure concepts and configurations provided by Window Server 2008. Students will be able to acquire a fundamental understanding in order to pursue advanced topics available for certification in the network and applications infrastructure areas.This training class is intended for new IT employees or  more...
MOC 5115 - Installing and Configuring the Windows Vista Operating System ... configure Windows Vista desktops.It focuses on four main areas: installing, securing, networking, and browsing. By the end of the class, the student will have installed and configured a Windows Vista desktop that is secure, on the network, and ready for browsing.This is the first course in the Windows Vista curriculum and will serve as the entry point for other Windows Vista Technology  more...
MOC 5116 - Configuring Windows Vista Mobile Computing and Applications This Windows Vista training class provides students with the knowledge and skills to successfully configure mobile computers and applications that run Windows Vista.The class will also provide them with the knowledge and skills necessary to ensure successful configuration of the IT Pro tools and productivity applications that ship with Windows Vista.Students will focus on six main areas:  more...
From GlobalCompliancePanel
New Final HIPAA Amendments New final rules for HIPAA Expand the Scope and Increase Responsibilities on-line e-learning cbt (computer based) ... changes into how they do business in their facilities. Areas Covered In the Session: The new regulations will be reviewed and their effects on usual practices will be discussed, as well as what policies need to be changed and how. We will show what policies and evidence you need to produce if you are audited by the HHS Office of Civil Rights. Now that there is a legislative mandate to  more...
Risk Management in IEC 60601-1 Third Edition - Webinar By GlobalCompliancePanel ...be understanding the requirements of the new standard. Areas Covered in the Session: ISO 14971 compliance is a requirement of IEC 60601-1 The new standard uses risk management throughout The new standard is less prescriptive in many areas The new standard requires that all applicable collateral and particular standards must be used for compliance Current activities leading to full  more...
FDA 483 Observations in the Laboratory What went wrong How can they be avoided - Webinar GlobalCompliancePanel In order to proactively address areas of concern to the FDA and other regulators, All units within each pharmaceutical firm should review recent regulatory observations and proactively establish programs or systems to address the regulatory concerns. Tuesday, January 10, 2012 10: 00 AM PST | 01: 00 PM EST  more...
Medical Coding for Dental Sleep Apnea Treatment - Webinar By mentorhealth This webinar will provide the information that dental practices need to be able to truly help their patients afford this life saving treatment. All areas of helping dental practices implement this profit boosting system will be discussed. Price List: Live : $195. 00 Corporate live : $695. 00 Recorded : $245. 00 webinars@mentorhealth. com Phone: 800-447-9407 Fax: 302-288-6884  more...
Clean Room Microbial Load and Characterization of Microorganisms in the Clean Room Environment - Webinar By GlobalCompliancePane A summary of test methods will be covered, and a review of types of microorganisms that can be present, will be discussed. A general review of environmental niches where they may be present will be discussed. You will be introduced to the different methods available to conduct testing. Key areas discussed will be Compressed Air, Personnel Monitoring, Surface and Raw Material Monitoring.  more...
Calculating Overtime Correctly - Webinar By TrainHR ...ert Vicki M. Lambert in this information packed event! Areas Covered in the Session: How to calculate the regular rate of pay The eight narrowly construed exceptions to inclusion of payments in the regular rate When you must include a bonus in calculating your employeea ™s overtime pay How to handle overtime calculations once you've determined that a bonus qualifies as  more...
Introduction to Contamination Control Master Plans - By GlobalCompliancePanel ... risks of the specific contaminants for your products. Areas Covered in the Session: What is a CCMP and how is it valuable to my company? What topics are covered in the CCMP and to what extent? How is the CCMP controlled and updated? How is the CCMP implemented? Who contributes to the CCMP? Who Will Benefit: QA personnel Regulatory personnel Operations managers Microbiologists R&D  more...
From ZaranTech.com
SAP FICO Online Competency Development Training program ...7. Screen Layout- Asset class/ Asset master/ depreciation areas 28. Depreciation Keys: Define Base Method/ Define Multi level method/ Period control methods 29. Creation of main Asset master and sub asset master data/ Asset transactions 30. Depreciation run/ display of balances 31. Reports and Integrations 32. Financial statement versions/ Reports in G/ L accounting/ list of accounts/ List  more...
From GlobalCompliancePanel
A Simpler Approach to Implementing or Validating CGMPs to 21 CFR 11 Electronic Records Signatures - Webinar By GlobalComplianceP ...a ™s resource constrained industrial environment. Areas Covered in the Session: Verification or Validation Current Regulatory Expectations and Recent Audit "Hot Buttons" The Part 11 Project Validation Plan The Simplified Approach to 21 CFR Part 11 Compliance and Software V&V When and How to Use DQ, IQ, OQ, PQ (or their equivalents) Simplified Sample V&V Test Cases and their  more...
Practical Laboratory Statistics This presentation will attempt to remove the fear of statistics that most people share. We will not spend much time on complex equations. Rather, we will focus on the concepts of statistics, and how you can use these concepts to interpret your laboratory results. Our focus will be on using basic spreadsheet functions to compare data sets generated from many different kinds of test equipment.  more...
Validating Radiation Sterilization for Medical Device Industries by gcp ... may be incorporated into the design inputs correctly. Areas Covered in the Session: Introduction Terminology / Definitions Radiation characterization / effectiveness Process Equipment Product and Material Issues Process Definition Validation IQ/ OQ/ PQ Documentation, review and approval of validation Routine Monitoring Product Release Maintenance of process effectiveness Who  more...
Assessing Unemployment Insurance Cost Controls by Train HR This webinar discusses the purposes and methodologies of UI audits in assessing an organization's unemployment insurance controls and the use of UI audits in reducing the organization's UI risk exposure and lowering UI tax liabilities and costs. Critical areas of UI cost management are reviewed and effective cost control strategies are identified.  more...
Breakthrough Performance Management that is Practical Effective and User-Friendly ...ntation, but do not help with performance improvement. Areas Covered in the Session: Performance Management How to Give Feedback Coaching Counseling How to handle personnel problems How to improve performance of subpar employees How to define good performance How to develop employee potential Who Will Benefit: Managers Supervisors  more...
The Law and Psychology of Mental Health Issues at Work Substance Abuse Depression and the Bermuda Triangle of the ADA the FMLA a ...his costs organizations millions of dollars each year, Areas Covered In the Seminar: How the ADA, FMLA and Workers' Comp intersect When do conduct problems become mental illness? What do you say to a depressed employee? What protection do alcoholics and substance abusers have under the A. D. A. How to handle threats and other disruptive behavior The 5 biggest mistakes managers make in  more...
Document Retention and Destruction ...owing you are prepared for any audit of your records. Areas Covered in the Session: Where records should be kept What belongs in a personnel file Keeping and maintaining legal records Payroll and taxes Back- up systems Critical incidents files Documenting oral and electronic communications Security of files Archive methods and back-up systems Who Will Benefit: Chief Human  more...
Valuing and Understanding Diversity in the Workplace Today by TrainHR ...ifferent aspects of a diverse workforce. We will cover areas of sensitivity and inclusion as well as legal considerations for protected classes and the business case for diversity. We will explore assumptions, beliefs, generalities, discrimination, prejudice, perception, and stereotypes. We will cover changing demographics and top growth groups, generational diversity, gender differences,  more...
Bullying in the Workplace by TrainHR ...ifferent aspects of a diverse workforce. We will cover areas of sensitivity and inclusion as well as legal considerations for protected classes and the business case for diversity. We will explore assumptions, beliefs, generalities, discrimination, prejudice, perception, and stereotypes. We will cover changing demographics and top growth groups, generational diversity, gender differences,  more...
How to Create Configure and Manage a Design Inputs - Design Outputs Traceability Matrix utilizing the principles of Lean Documen Design Inputs, Design Outputs, and Traceability matrices present a challenge to almost all industries that apply design controls. Typically, these cause the creation and maintenance of duplicate information across various documents - a major source of errors. This webinar applies the Theory of Lean Documents and the corresponding Theory of Lean Configuration to avoiding these errors, while  more...
Creation and management of a Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Controlled documents are one of the foundational building blocks of a Quality Management System (QMS) for regulated industries. Too often, controlled documents are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed. This webinar applies the Theory of Lean Documents and the corresponding Theory of Lean Configuration to this key part of a QMS.  more...
Creation and configuration of a Equipment Facilities and Preventive Maintenance System utilizing the principles of Lean Document Proper preventive maintenance and management of process equipment, and facilities is the foundation for any manufacturing process, including many processes not typically thought of as manufacturing.  more...
Creation of DHFs DMRs and DHRs utilizing the principles of Lean Documents and Lean Configuration by GlobalCompliancePanel Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are key building blocks used in the design, development, manufacturing, and cGMP compliance for the Medical Device Industry. Too often, these are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed. This webinar applies the Theory of Lean Documents and also  more...
HIPAA Enforcement and Compliance Audits What the auditors want and how to be ready before they call - Webinar By GlobalComplianc ...udit and respond to an audit request will be outlined. Areas Covered in the Session: * Fines and penalties for violations of the HIPAA regulations have been significantly increased and now include mandatory fines for willful negligence that begin at $10, 000 minimum. * HIPAA Audits have been few and far between in the past, but that's now changing - the HHS will be auditing HIPAA  more...
Good Documentation Practices for Laboratory Operations - Webinar By GlobalCompliancePanel ...ces apply to all pharmaceutical manufacturing and support areas. Good Documentation Practices describe the required activities and steps to use when recording data and other handwritten entries. Personnel, who work with documentation must be informed of these requirements, recognize their significance to their job and be aware of the consequences of non-compliance. During this webinar, you will  more...
DHF DMR DHR Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel ...nd desirable contents will be discussed. Also considered: Areas requiring frequent re-evaluation / update; Similarities and differences; Future trends; Typical DHF Table of Contents; Technical File or Design Dossier Table of Contents; The importance and usefulness of the "Essential Requirements"; Structure of the "Declaration of Conformity"; self-declaring or N-B reviewed; Parallel approaches  more...
HIPAA Security Policies and Procedures Making them useful and relevant as well as compliant - Webinar By GlobalCompliancePanel ...ure for the set of policies needed and identify the topic areas that policies should include, making it easier to deal with the dozens of policy details that are required. Areas Covered in the Session: * Find out what are the requirements for policies and procedures and why they're a good thing. * Learn how having good policies and procedures and good documentation can make  more...
Information Security and Payment Card Rules Protecting Patient Payment Data and Complying with PCI - Webinar By GlobalCompliance ... security policies meeting HIPAA and PCI requirements. Areas Covered in the Session: * Health and payment information must be kept securely - learn what is required and what is a good way to attain compliance with multiple regulations * HIPAA and PCI have many similarities, but some important differences as well. Keeping your information well controlled can help with both. *  more...
Information Security Risk Analysis Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePane ...ance from the US Department of Health and Human Services. Areas of high risk, as identified by respected industry organizations, will be identified to ensure that the most significant risks are discovered and adequately prioritized. The risk analysis process will be applied to a simplified example in order to relate the process to a real situation and drive home the usefulness of the  more...
The GCPICH Obligations of Sponsors Monitors and Investigators - barriers and solution - Webinar By GlobalCompliancePanel ...sora ™s / CROa ™s Monitors are so important. Areas Covered in the Session: * The historical background of why the GCP standards were developed * The concept of and the purpose of a GCPa * The thirteen ICH Principles of a GCPa * The ICH definition of a GCPa and how it is applied * The Regulatory requirements to follow to be GCP compliant *  more...
Pharmaceutical and Medical Device Validation Guidances - Similarities and Differences - Webinar By GlobalCompliancePanel ...edictable manner to treat, cure, and diagnose disease. Areas Covered in the Session: * Defining IQ/ OQ and validation and its role in maintaining product quality * Roles and responsibilities in the validation process * The process validation lifecycle from design to product discontinuation * How about Process Analytical Technology (PAT) * Similarities and  more...
Auditing an Active Pharmaceutical Ingredient API Contract Manufacturing Organization CMO - Webinar By GlobalCompliancePanel ...establish with a CMO is critical to your supply chain. Areas Covered in the Session: * Examine key elements of an API audit * Audit preparation * The audit itself o Opening Session o Audit itself o What to look for? o Discussion of findings o Suggestions and experience * Closing Meeting * Who should participate  more...
Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel Overview: CAPA is the most audited Quality subsystem in any Quality system. Most of the warning letters written by the FDA in 2010 were CAPA relate. Avoiding FDA CAPA findings starts with the design of a robust CAPA SYSTEM. The webinar covers "Off-label statute" and the FDA's nonbinding off-label guidance as relates to re-prints, performance claims, and Promotion. Emphasis is placed on ethical,  more...
Develop and Execute the Company Software VV Program - Webinar By GlobalCompliancePanel ...a ™s resource constrained industrial environment. Areas Covered In the Session: * Verification or Validation * Current Regulatory Expectations and Recent Audit "Hot Buttons" * The Project Validation Plan * Product and Process / / Facilities / Equipment Software V&V * When and How to Use DQ, IQ, OQ, PQ (or their equivalents) * GAMP / Other Considerations  more...
Root Cause Analysis - The Heart of a Successful CAPA Program - Webinar By GlobalCompliancePanel ...Systems / cGMP planning, implementation and execution. Areas Covered In the Session: * Regulatory "Hot Buttons" * The 4 Basic Steps to Problem Solving * A Suggested Investigation Template * ID / Document the Problem * Investigation / Analysis Methodology - The 7 RCA "Tools" * Find the Solution(s) * Monitor for Effectiveness * Lock In the Change -  more...
Developing the Master VV Plan to Meet US FDA ISO 13485 and 14971 Requirements - Webinar By GlobalCompliancePanel ...ience, but proper up-front V&V planning and execution. Areas Covered In the Session: * Verification or Validation - Recent regulatory expectations * The Master Validation Plan / structure * Product Validation a how it differs from process / equipment V&V * Process / Equipment / Facility Validation - FDA's new guidance * When and How to use DQ, IQ, OQ, PQ, or  more...
Recalls Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel ...magazines, newspapers available to firms' competitors. Areas Covered in the Session: * Complaint definitions - FDA, Canada & Europe * FDA's complaint handling requirements * Canada & European Union complaint handling * FDA's voluntary & mandatory reporting * 21CFR 803, 806 & 810 explained * FDA regulatory actions against firms * Adverse event reporting -  more...
FMEA and Risk Management for Medical Devices - Webinar By GlobalCompliancePanel ...ufacturers and has been replaced by "Risk Management". Areas Covered in the Session: * Failure Mode Analysis Terms * Risk Management and FDA * Risk Management in Design Control * Risk Management & ISO 14971 * Risk Management in Design Control * Risk Management & ISO 14971 * Risk Management & Medical Device Directives Who Will Benefit: *  more...
21 CFR Part 11 How to Successfully Prepare for and Host an FDA Inspection - Webinar By GlobalCompliancePanel ...organization shall comply with the Part 11 regulation. Areas Covered in the Session: * Short and quick overview of the Part 11 regulation * Detailed description of HOW TO prepare for an FDA inspection * When and Where Part 11 is in scope or the scope of the inspection; * Detailed description of HOW TO handle the FDA inspection during the inspection itself; * Some  more...
Internal 21CFR Part 11 Compliance Auditing of Computer Systems - Webinar By GlobalCompliancePanel ...ady for an internal QA or FDA inspection at your site? Areas Covered in the Session: * 21CFR Part 11 Compliance * Review of the regulations * Regulatory requirements * Site Inventory * Compliance Assessment * Risk Assessment Who Will Benefit: The employees who will benefit include: * End-users responsible for applications that need to be validated  more...
Key Factors to Write an Effective Standard Operating Procedure SOP and Work Instructions WIs - Webinar By GlobalCompliancePanel ...perating procedure is, and what a Work Instruction is. Areas Covered In the Session: * How to write a work instruction * How to write a standard operating procedure * Properties of an effective work instruction * Properties of an effective Standard operating procedure * The differences between work instructions and Standard operating procedures. Who will  more...
Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ...tion and testing data and maintaining them in the DHR? Areas Covered in the Session: * FDA Quality Systems Regulation Requirements/ Definitions * MDD Requirements/ Definitions * Design History File (DHF) o Definition o Typical contents o DHF and outsourced design/ production o DHF and OEM relationships * Device Master Record  more...
Conducting Successful Product Complaint Investigations - Webinar By GlobalCompliancePanel ...est practices for timely and effective investigations. Areas Covered in the Session: * Understand how and why CAPA is tied in to product complaint investigations * Examples of tools currently being used to conduct investigations * How far and in-depth do you go with your investigations * What are current FDA "hot" buttons and trends * Benchmarks and best practices  more...
The Most Common Problems in FDA Software Validation Verification- Webinar By GlobalCompliancePanel ...ir ability to improve the level of validation success. Areas Covered In the Seminar: * Outline of FDA regulations as applied to software. * Review of FDA software validation requirements. * Why validation makes good business sense. * Most Common Problems in FDA Software Validation & Verification. * Strategies on how to avoid the most common problems. * Advice  more...
How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel ... * Learn how to better audit quality record systems. Areas Covered in the Session: * Introduction * Guidance documents/ QS regulation * Major FDA 483 points * Trends in FDA warning letters * Determining best practice for the DHR audit * Be prepared by knowing how to conduct a MORE thorough record audit * FDA 483 point issuance prevention Who Will  more...
Data Security Analysis for Healthcare Providers - Webinar By GlobalCompliancePanel ... risk analysis and meet HITECH and HIPAA requirements. Areas Covered in the Session: * "Meaningful Use" data security analysis requirements * HIPAA risk analysis requirements * Methods for building a customized analytical tool * Questionnaires and forms Who Will Benefit: * Healthcare providers * Healthcare privacy officers * Healthcare security  more...
Webinar on Cloud Computing SaaS - Webinar By GlobalCompliancePanel ...e you need to maintain a validated cloud based system. Areas Covered in the Session: * The difference between the Conventional Implementation and a Saas Implementation Methodology * When requirements can be limited to Customer specific configurations * When the Customer specific configuration can be validated rather than the full system. * When Vendor SOPs can be  more...
Understanding Attribute Acceptance Sampling including Z14 and c0 Plans -- Webinar By GlobalCompliancePanel ... have heard about? * Can you improve the process? Areas Covered in the Session: * Sampling concepts o With or without replacement o Simple or stratified sampling * The binomial distribution o Possible outcomes and Bernoulli trials o The binomial formula and what it means o The cumulative binomial * Sampling plans  more...
Requirements of the Master Production Record - Webinar By GlobalCompliancePanel ...equirements for the master production records. Applicable areas may include clinical, technology transfer, and routine manufacturing and packaging for the API and finished commercial product. It is the intent of this program to enable your firm to have a consistent, compliant approach and maintain continuous improvement in the area of production records. With the information gained from this  more...
Best Practices for the Implementation and Use of Test Management Tools - Webinar By GlobalCompliancePanel ...nce requirements and Automated Testing considerations. Areas Covered in the Session: * System Based Test Tools vs. Paper Based Test Tools * Paper Based Validation Practices vs. System Based Test Tools * Test Management Tool Implementation Considerations * Test Management Tool Usage Considerations * Automated Testing Considerations Who Will Benefit: * IT  more...
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP ...ta integrity, oversight of investigators as well as other areas. The components of a quality monitoring system will be presented so that participants can assess their current practices for identifying gaps and risks, particularly in relation to preparing for regulatory inspections. It will be important to see what the FDA regulations and the ICH GCP recommendations are in this regard. The  more...
Gowning Systems Used in Cleanrooms Controlled Environments - Webinar By GlobalCompliancePanel ...r to establish a consistent manufacturing environment. Areas Covered in the Session: * Identify what garment systems are available. * Identify and discuss good and bad cleanroom gowning. * Identify gowning techniques and sequence. * Discuss what role each garment part plays in contamination control and human safety. * Explore expectations of cleanroom garment  more...
Facilities Cleaning in Cleanrooms and Controlled Environments - Webinar By GlobalCompliancePanel ...ning processes and ensure best practices are followed. Areas Covered in the Session: * Learn about cleaning and what it accomplishes in the cleanroom. * Identify cleaning agents, tools, and equipment. * Discuss cleaning personnel training and qualification. * Identify the methods of cleanroom cleaning. * Identify and discuss extent and frequency of cleanroom  more...
Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel ...* Allocating Analytical Instruments to USP Categories Areas Covered in the Session: * Operational lab equipment requirements for calibration and qualification * Most common inspection problems * USP Chapter : Analytical Instrument Qualification * Development of an effective equipment qualification master plan * Calibration/ qualification phases: design  more...
The Use and Mis-use of FMEA in Medical Device Risk Management - Webinar By GlobalCompliancePanel ...ing efforts toward the real value of the FMEA process. Areas Covered in the Session: * What is an FMEA o What are the components of an FMEA? * How should I use FMEA in performing risk management? * What are the problems with FMEA in risk management? * How is an FMEA conducted o What and who are needed o Identifying significant risks  more...
Understanding ISO 13485 vs ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel ...h analysis of ISO 13485 with comparisons to ISAO 9001. Areas Covered in the Session: * Principles of ISO 13485: 2003 * ISO 9001 & ISO 13485 Differences * Risk Management & ISO 14971 * FDA's MDR's & EU Vigilance * Design Control * MDD 93/ 42/ EEC & Essential Requirements Who Will Benefit: * Manufacturing & Design Engineers * Marketing Product  more...
Good Documentation Practices for GMP Operations - Webinar By GlobalCompliancePanel ...ces apply to all pharmaceutical manufacturing and support areas. Good Documentation Practices describe the required activities and steps to use when recording data and other handwritten entries. Personnel who work with documentation must be informed of these requirements, recognize their significance to their job and be aware of the consequences of non-compliance. During this 1-hour webinar, we  more...
The Pharmaceutical Quality System - Webinar By GlobalCompliancePanel Overview: This webinar will discuss the evolution of the standards, describe a Pharmaceutical Quality System and discuss the transition to the Pharmaceutical Quality System. Why you should attend: The US FDA, and regulatory agencies around the world, are actively promoting the concept of a Pharmaceutical Quality System. The concept of a Quality System was imposed on the medical device industry  more...
A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - W ...earning experience. Questions are strongly encouraged. Areas Covered in the Session: * Module 1 - Introduction to Quality and Compliance Concepts * Module 2 - Differences between Medical Devices and Pharmaceuticals * Module 3 - Scope of the GMPs and the Quality Cycle * Module 4 - Standards of Quality * Module 5 - The Shifting Paradigm to Focus on Customer and User  more...
Navigating the Regulatory Environment for the Implementation of Alternative Microbiology Technologies - Webinar By GCPanel ...onducting GMP audits at your manufacturing facilities. Areas Covered in the Session: * Review current regulatory status of rapid method acceptance * Regulatory publications and presentations focusing on RMM implementation * Current perspectives from the U. S. Food and Drug Administration (FDA), European Medicines Agency (EMA), Australian Therapeutic Gods Administration (TGA)  more...
Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel ...d in compliance with sound quality management systems. Areas Covered in the Session: * Compilation of Completed Records * Quality Technical Agreements * QA review of production records * Laboratory Testing Results * Batch Production Record Review * Critical Utilities and Environmental Monitoring Data * Requirements for COA * Communication * Lot  more...
Controlled Substances and the Hospital Pharmacy - Webinar By GlobalCompliancePanel ...bstance. Objectives of the Presentation: The following areas are covered: * DEA Office of Diversion Control: This section will familiarize you with the authority given to DEA Diversion Group when enforcing the laws and regulations pertaining to controlled substances and regulated chemicals. * Controlled Substances Act: Briefly describes the criminal and civil actions that can be  more...
Validation of ExistingLegacy Computer Systems for FDAEU Compliance - Webinar By GlobalCompliancePanel ...hecklist: Retrospective Validation of Computer Systems Areas Covered in the Session: * Definition of legacy systems and retrospective validation * FDA requirements and inspection practices * Examples of FDA warning letters * Industry recommendations, e. g., from the GAMP * Assessment activities, e. g., gap analysis and risk assessment * Reviewing and updating  more...
HIPAA Business Associates How the regulations have changed and what you need to do for compliance now - Webinar By GCPanel ...mandatory penalties for willful neglect of compliance. Areas Covered In the Seminar: * Learn about the new requirements for HIPAA Business Associates * Find out what has changed for Business Associates * Learn how the definition of BA has been significantly expanded * Learn what goes into a proper Business Associate Agreement * Find out about the new, higher  more...
HIPAA Breach Notification What to do to prevent breaches and what to do when they happen to you - Webinar By GCPanel ...ncidents and breaches to withstand enforcement audits. Areas Covered In the Seminar: * Learn about the HIPAA Breach Notification Rule * Find out what is a breach * What to do to prevent a Breach * What to do to prepare for a Breach * What to do when a Breach occurs * What you have to report, to whom ,and when * How to avoid Breach Notification Agenda:  more...
Off-Label Promotion of Medical Devices Maximizing Your Performance Claims within FDAs Framework of Acceptable Practices - Webina Overview: The webinar covers "Off-label statute" and the FDA's nonbinding off-label guidance as relates to re-prints, performance claims, and Promotion. Emphasis is placed on ethical, moral, and legal expectations from the FDA. You will improve your understanding of regulatory expectations for your products and improve promotional compliance for released products. The webinar is designed to  more...
Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel Overview: The webinar examines critical parts of design control after product release including: design change control, design validation, and the Design History File. The webinar is designed to help regulatory Affairs, Quality Engineers, and Design Engineers maintain released products within current regulatory requirements. As an attendee you will learn what the FDAs expectations for your  more...
Regulatory Complaint Handling Vigilance Recalls - Webinar By GlobalCompliancePanel Overview: Improper complaint handling can result is serious regulatory problems as well as hitting the bottom line. Recalls, FDA Warning letters & even seizures could result. This presentation will review the regulatory requirements for complaint handling and adverse events reporting in the USA, EU & Canada. Suggestions for investigating and documenting complaints & pitfalls will be included.  more...
Overall Residual Risk Evaluation - Webinar By GlobalCompliancePanel ...ce on how to perform Overall Residual Risk Evaluation. Areas Covered in the Session: * Choosing the Evaluation Team * Determining the Evaluation Process * What documents should be part of the review? * Using the Risk Chart in the review * How to compare to the Risk Acceptability Criteria * Documenting the results of the Evaluation Who will benefit: *  more...
Documentation for IEC 60601-1 3rd Edition Compliance - Webinar By GlobalCompliancePanel ...ation process as well as additional time requirements. Areas Covered in the Session: * Requirements of IEC 60601-1 Third Edition * Required use of Collateral standards * Required use of Particular standards * Required use of ISO 14971 Risk Management * Use of IECEE Test Report Forms Who will benefit: * Compliance Engineers * Project Managers *  more...
Developing the Risk Management Plan - Webinar By GlobalCompliancePanel ...ent and manufacturing activities are located in different areas and are under different management structures, the Risk Management Plan must document the divided responsibilities and activities. The plan must cover all phases of the product lifecycle risk management activities. This presentation will discuss how to accomplish risk management planning in divided management structures. Why you  more...
FDAs New Process Validation Guidance - Webinar By GlobalCompliancePanel ...now demanded by FDA with the release of this standard. Areas Covered in the Session: * Specific discussions include * Background of the original guidance, its history, application, and items covered * FDA regulatory authority * Growth of competing standards and the competing expectations of the medical device industry * The history and philosophy of the new  more...
Validating Rapid Microbiological Methods - Webinar By GlobalCompliancePanel ... Eur. Chapter 5. 1.6 and the PDA Technical Report #33. Areas Covered in the Session: * Learn how to develop a validation strategy * User requirements specifications (URS) * Design Qualification (DQ) * Supplier assessment/ audit * Functional design Specifications (FDS) * Requirements Traceability Matrix (RTM) * Developing test plan, including installation,  more...
Excel Spreadsheets Step-By-Step Instructions for Compliance - Webinar By GlobalCompliancePanel ...ke you a better Excel user, saving you time and costs. Areas Covered in the Session: * Develop spreadsheet applications that are GxP compliant. * Avoid 483s and warning letters. Critical data, such as laboratory information and other GxP data, is often recorded in spreadsheet applications and are subject to regulatory inspection. * Learn how to use Excela ™s built in 21  more...
Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel ...ence will prepare you to perform a validation project. Areas Covered in the Session: * Learn which documents the FDA expects to audit. * How to use the risk-based validation approach to lower costs. * How to link requirements, specifications, risk management, and testing. * Document a computer system validation project using easy to understand fill-in-the-blank  more...
The Investigation System Discovery Planning Root Cause Analysis CAPA - Webinar By GlobalCompliancePanel ... effective root cause analysis for corrective actions. Areas Covered in the Session: * Elements of a thorough investigation process (Discovery through Closeout) * Identifying the Problem * Introduction to Root Cause Analysis * Define corrective action and preventive action * Effective Documentation of the Investigation Process * Skills and Tools of an  more...
Recruiting is Critical to Your Success What is the Secret - Webinar By GlobalCompliancePanel ...e right CRO or research site to conduct their studies. Areas Covered in the Session: * How to set up and track your recruiting of subjects * The challenges of successful recruiting * The importance of your recruiting staff in the overall success of the unit or site * How to build a data-base of patients * How to recruit more efficiently for a target study *  more...
Understanding the Calibration Curve - Webinar By GlobalCompliancePanel ...is presentation will help to eliminate these problems. Areas Covered in the Session: * Calibration Basics * Types of Calibration - External standard, Internal standard, etc. * Calibration Options - Response factor methods, Linear regression * Evaluation of Data - Three tools for evaluating regression data * Discussion using real-world data sets Who Will Benefit:  more...
Food Drug Cosmetic Act Implementing Regulations Major New Laws - An Overview - Webinar By GlobalCompliancePanel ...he Food Safety Modernization Act will also be covered. Areas Covered In the Seminar: * History of the Food, Drug & Cosmetic (FD&C) Act * Amendments to the Food, Drug, & Cosmetic Law * Overview of Major Regulatory Actions Since the FD&C Act: o Fair Packaging & Labeling Act o OTC Drug Review - Development of OTC Monographs o Tamper Resistant  more...
Design Control for Medical Devices - Webinar By GlobalCompliancePanel ...haps this deficiency extends to other systems as well. Areas Covered In the Seminar: * History of design control * Design planning * Design input/ output * Design reviews * Design documentation * Design transfer * In-process design control Who will benefit: This webinar will provide valuable assistance to all companies that perform design activities.  more...
Process Validation for Medical Devices - Webinar By GlobalCompliancePanel ...t can occur which may impact safety and effectiveness. Areas Covered In the Seminar: * What is Validation? * When should it be used? * How does it differ from verification? * Validation vs. Verification: Which One? * Protocol preparation * Different types of validation * IQ, OQ, and PQ Who will benefit: This webinar is targeted toward professionals  more...
How to use QSIT to Your Advantage - Webinar By GlobalCompliancePanel ... for? Even a thorough internal audit may not focus on the areas that the FDA inspector will. The most effective way to increase the likelihood of your internal audits identifying issues that the inspector will see is to arrange your internal audit scheme to mimic the process the FDA inspector will use. If you perform your internal audits this way, you'll be well prepared for the FDA. Areas  more...
Purchasing and Supplier Controls in the Medical Device Industry - Webinar By GlobalCompliancePanel ...if you have a great supplier control program in place. Areas Covered In the Seminar: * How to qualify new suppliers in a cost efficient manner * How to assess current suppliers in a cost efficient manner * How to perform supplier-related corrective action * Minimum documentation requirements for supplier qualification, assessment, and related corrective action Who  more...
Preparing for Pre-approval Inspections - Webinar By GlobalCompliancePanel ...reviewed followed by a detailed look at common focus area areas of Inspectors. Procedures to be followed after the inspection such as preparation of the response to 483s will be discussed. Ample discussion time will be available at the halfway point in the webinar and again at the end of the webinar. Why you should attend: Pre-approval inspections provides a relatively narrow window of time  more...
Best practices for conducting OOS investigations - Webinar By GlobalCompliancePanel ...ns face practical difficulties in complying with them. Areas Covered In the Seminar: * FDA requirements for handling OOS/ OOT results * Phase I- Laboratory Phase of Investigations * Phase II a Full Scale Investigation * Concluding an Investigation * Out-of Trend investigations * Common pitfalls during OOS Investigations * Review of recent OOS related  more...
Does your Equipment Program meet current regulatory expectations - Webinar By GlobalCompliancePanel ...am is also an expectation in GLP and GMP laboratories. Areas Covered In the Seminar: * FDA requirement for Equipment systems * Overview of GMP/ GLP requirements for equipment * IIQ/ OQ/ PQ of Equipment * Equipment database * Equipment SOPs * Equipment Calibration and maintenance * Review of equipment related citations in recent Warning Letters Who will  more...
FDAs Proposed Rule Regarding Device Establishment Registration and Listing and How to Register and List - Webinar By GlobalCompl ...tation regardless of the outcome of the Proposed Rule. Areas Covered In the Seminar: * When and how to register and list * Review the four proposed changes to FDA's device establishment registration and device listing regulations * Proposed changes to Implement the provision of Bioterrorism Act applicable to imported devices * Other proposed Amendments that would change  more...
Medical Device Recalls How to Manage Them and Recent Trends - Webinar By GlobalCompliancePanel ...potential risk to public health: Class I, II, and III. Areas Covered In the Seminar: * Create and use a recall operational procedure and what should it contain * Understand what are effectiveness checks * What happens in a medical device recall and your responsibility * Learn why a recall is either a correction or a removal depending on where the action takes place  more...
Off-Label Promotion of Drugs - Regulatory Documents Explained - Webinar By GlobalCompliancePanel ...nt tips to help companies prevent off-label promotion. Areas Covered In the Seminar: * Off-Label Use of Drugs * Overview of Current Legislation and Regulations * Recent Legal Actions * Pros and Cons to Permitting Off-Label Dissemination of Information * Recent FDA Guidance - Good Reprint Practices * Leveraging Requirements for Validation Who will benefit:  more...
Project Management for Clinical Trials - Webinar By GlobalCompliancePanel ...ther available information * Discuss the therapeutic areas with experts in the company and externally such as key opinion leaders, patient groups may also be of help * Decide on the study design potential locations for the study (eg which countries have a high incidence of the disease, where do you propose to market the drug * Identify potential locations for the study (eg which  more...
Meet FDA Expectations for a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel ...etting supplier buy-in. Coping with "rogue" suppliers. Areas Covered in the Session: * Regulatory "Hot Buttons" * Classify suppliers; Supplier requirements by "classification" * What's behind the COA? The COC? * The FDA's increasing emphasis on the site audit * Types of remote audits * Maintaining the relationship Who Will Benefit: * Senior  more...
Developing and Using the Product Risk Management FileReport - Webinar By GlobalCompliancePanel ...g tool, and how to maintain it as a "living document". Areas Covered in the Session: * The Revised ISO 14971: 2007 for Devices * ICH Q9 for Pharma * Product Hazard Analysis * Design, Process, and Use[r] Failure Mode, Effects and Criticality Analysis * Fault Tree Analysis * Suggested Risk Management File / Report, FMECA, FTA Templates * The Team and Its  more...
Change Control -- Your Companys GMP Weak Point - Webinar By GlobalCompliancePanel ...valuate their change control system and its impact on all areas of a companya ™s cGMP activities. Why you should attend: The last few years have seen an increase in product recalls. For this and other reasons, the U. S. FDA has come under increasing negative public scrutiny. High profile drug recalls, food chain problems and contamination, import problems, resignations. Now a new  more...
Tougher US FDA cGMP Compliance Audits - When Youre Not Ready - Webinar by GlobalCompliancePanel ...d, proactively address these trends, and start to address areas of known deficiencies. We will evaluate the chief areas of an FDA CGMP compliance audit to see actual and anticipated changes in emphasis based on this new regulatory climate. We will also discuss proven methods to prove to the FDA that known company cGMP deficiencies should not be a major concern to the Agency, and which may  more...
Introduction to Investment Risk - Credit Market and Portfolio - Webinar by GlobalCompliancePanel ...uding the major frameworks and standards in use today. Areas Covered in the Session: PART ONE - Market Risk After attending this session, you will be able to: * Differentiate between Qualitative and Quantitative Techniques * Apply Three Approaches to Value at Risk (VaR) * Understand the Limitations of VaR * Prepare for Black Swans PART TWO - Volatility, Risk  more...
Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel ...eate regulatory problems that are will be hard to fix. Areas Covered in the Session: * Overview of the regulations o Automated processes o Production and process changes o General record keeping requirements o Electronic records * Excel Validation o Setting the validation criteria + Data types  more...
Introduction to Contamination Control Master Plans - Webinar by GlobalCompliancePanel ... risks of the specific contaminants for your products. Areas Covered In the Seminar: * What is a CCMP and how is it valuable to my company? * What topics are covered in the CCMP and to what extent? * How is the CCMP controlled and updated? * How is the CCMP implemented? * Who contributes to the CCMP? Who will benefit: * QA personnel * Regulatory  more...
Cleanroom HEPA Filter Testing Certification An Owners Guide - Webinar by GlobalCompliancePanel ...and, interpret, and act on the results of the testing. Areas Covered In the Seminar: * Define cleanroom filters and equipment * Identify regulatory expectations and industry standards * Define the tests, frequencies, and methods * Define the expectations for testing equipment * Identify who does the testing * Identify requirements for documentation/ logs/  more...
Process Validation current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel ...ee practical examples of process validation protocols. Areas Covered in the Session: * Recent Guidance Documents * Industry Practices * Examples of Process Validation Protocols * What should be included in Process Validation Protocols * The Importance of Good Process Validation * Common mistakes in Process Validation Who Will Benefit: * Director of  more...
Understanding the Technical Requirements of 21 CFR Part 11 - Webinar by GlobalCompliancePanel ...requirements of 21 CFR Part and how to implement them. Areas Covered in the Session: * Leveraging a Part 11 Interpretation document * The Importance of Part 11 in Requirements and Specifications documents * The Role of Risk Assessment in Part 11 Compliance * Technical Controls for Electronic Records * The Many Flavors of Audit Trails * Open vs. Closed Systems  more...
International Financial Reporting Standards The Basics - Webinar by GlobalCompliancePanel ...consist of, and what these changes mean for companies. Areas Covered in the Session: * GAAP vs. IFRS * What will change * What will not change * Who needs to comply * The four key principles of IFRS * How disclosure requirements will change * The new rules for assigning values to assets * The deadlines for adoption * How IFRS will affect SOX  more...
Practical Laboratory Statistics - Webinar by GlobalCompliancePanel Overview: This presentation will attempt to remove the fear of statistics that most people share. We will not spend much time on complex equations. Rather, we will focus on the concepts of statistics, and how you can use these concepts to interpret your laboratory results. Our focus will be on using basic spreadsheet functions to compare data sets generated from many different kinds of test  more...
Effective Corrective and Preventive Actions CAPA 10 Steps to Success - GlobalCompliancePanel Virtual Seminar - Webinar By Global ...which can be immediately applied in your organization. Areas Covered in the Seminar: * Module 1 o Introduction and Overview o Correction vs. Corrective Action + Understanding of all elements of CAPA process step as required by ISO and regulatory agencies + Introduction to CAPA elements in a practical and proven manner which can  more...
21 CFR Part 11 Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar - Webinar By GlobalCompliancePanel ...r best friends and/ or worst enemies at the same time. Areas Covered in the Seminar: * Module 1 - Overview and Understanding of the Regulation o Introduction and development of the regulation o What to expect in the future when it comes to the regulation o Options for (non)compliance o 'What ifs' o Most impactful sections and  more...
Reprocessing REUSABLE Medical Devices-Cleaning Labeling Requirements - Webinar By GlobalCompliancePanel Overview: Much attention has been paid to the regulatory requirements of reprocessing SINGLE use devices. However, there is increasing attention being directed towards reprocessing REUSABLE medical devices and regulatory requirements. The purpose of this seminar is to explain the rationale, the legal requirements and some methods commonly used for reprocessing & validating reusable medical  more...
Food Safety Management Systems - ISO 220002005 - Webinar By GlobalCompliancePanel ...the international standard for Food Safety Management. Areas Covered in the Session: The following areas will be addressed: * Key terms and definitions * General Requirements * Documentation * Management Responsibility * Resource Management * Planning and Realization of Safe Products a flow diagrams, process steps and control measures * Hazard  more...
Controlled Substances and the Pharmacist - Webinar By GlobalCompliancePanel ...nd security responsibilities placed on the pharmacist. Areas Covered in the Session: * Discuss the types of federal criminal and civil actions that can be imposed on a pharmacy pertaining to the purchase, sale, transfer, dispensing, destruction and theft or loss of Schedules II through V controlled substances. * Identify the responsibilities of DEA through their Diversion  more...
Hazard Analysis vs FMECA Differences and Commonalities - Webinar By GlobalCompliancePanel ...ifferent product development phases will be discussed. Areas Covered in the Session: * Hazard analysis techniques * FMECA techniques * Probabilistic approaches * When to use which method during the design process * Effective evaluation strategies and documentation formats Who Will Benefit: * Project Managers * Regulatory Affairs * System  more...
Labeling Requirements for Dietary Supplements - Webinar By GlobalCompliancePanel ... in regulatory fines * Improve your profitability Areas Covered in the Session: * Labeling defined * Current compliance labeling issues * Labeling requirements * How to design a labeling program that is compliant * How to audit your labeling program for compliance Who Will Benefit: * VP Quality * Manager of Quality * CEO of dietary  more...
Medical Device Changes and The 510k - Webinar By GlobalCompliancePanel ...ed into action in the past year will provide direction in areas of concern and what to expect in the future. This will be performed by a review of FDA-stated areas of required review and a suggested matrix format. Anticipation and addressing such on-going product modifications / changes proactively will further prove a company is "in control", and assist documenting the 510(k) submission (or  more...
Validating Excel and Word Applications Documents - Webinar By GlobalCompliancePanel ...imate that has resulted in this call for change, and flag areas for heightened compliance in V&V planning. It will focus on eliminating major systemic validation problems. It will assist the attendee to review their existing system in light of current and anticipated changes in regulatory thinking, and in approaches to implementing necessary changes, in a realistic, risk-based approach. Why  more...
Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel ...th the FDA. Use them to prove "progress against plan". Areas Covered in the Session: * Why formal Project Management * The three most common tools * How to compile * Gantt, CPM, PERT * Simple construction techniques * Work breakdown Structure, Milestones, Tasks * Effectiveness - Determining and Monitoring * The "New Product Example" * The  more...
Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanel ... contributes to performance, it must be done properly. Areas Covered in the Session: * Review of GMP regulatory expectations of training (FDA and EU) * Recent training-related citations * High-Level description of a training system, including elements (needs analysis through evaluation), basic training documentation, management, GMP training plans/ planning, and trainers  more...
Legal Risks in Social Media for Healthcare Providers - Webinar By GlobalCompliancePanel ...need to ensure that they are focusing on the correct risk areas and structuring their social media activities in ways that allow them to effectively operate a social media marketing program. Areas Covered in the Session: * Legal issues from the public's perspective * Legal issues from the organization's perspective * HIPAA issues impacting social media marketing *  more...
Preparing for GFSI and other Third Party Audits - Webinar By GlobalCompliancePanel Overview: Preparation and organization are the keys to a successful audit. This session will allow your team to anticipate the auditors needs and result in the facility's ability to achieve the maximum benefit and score from the audit. Why you should attend: More and more customers are requiring GFSI audits such as ISO 22000, BRC and SQF or accepting them in lieu of their own audits.  more...
Chemical Control for Food Manufacturers Ingredient Cleaning and Hazardous Materials - Webinar By GlobalCompliancePanel Overview: A comprehensive review of an ideal chemical control program will be presented. The guidelines presented will enable your company to implement programs that are cost effective and meet or exceed the expectations of major QSR, and GFSI audit criteria. This presentation will provide not only a provide schematic for management and control of chemicals, but an interactive and customizable  more...
Why is CAPA so often cited in medical device inspections - Webinar By GlobalCompliancePanel ...management subsystems to be reviewed by investigators. Areas Covered in the Session: * Review CAPA citations in FDA-483 and Warning Letters * Identify common problems with CAPA * Identify FDA CAPA regulatory requirements * Identify ISO 13485 CAPA requirements * Explore FDA's risk expectations of CAPA systems * Establishing a risk-based CAPA system Who Will  more...
Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - Webinar By GlobalCompliancePanel ...e integrated with the CAPA and Change Control Systems. Areas Covered in the Session: * What should be investigated - Complaints, audit observations, deviations, discrepancies, calibration out-of-tolerances * FDA expectations for investigations * The investigation-problem resolution process - understand the problem, identify possible causes, data collection, data analysis,  more...
Using Foreign Trial Data in Your NDA Approval Process - Webinar By GlobalCompliancePanel ...bmissions accepted by FDA - mainly in limited therapeutic areas. Given lower costs and shorter recruiting times, the use of foreign sites is appealing to all drug developers, especially generic and 505(b)(2). Due to shortcomings found during site inspections, lack of inspection resources and the general tightening of FDA safety reviews, FDA has started imposing some a unwrittena requirements  more...
Complying with HIPAA Security Rules Whats in the rules and how you can most easily prepare for compliance - Webinar By GlobalCom ...and avoid violations and penalties for non-compliance. Areas Covered In the Seminar: * Learn what kinds of entities are now covered under the HIPAA Security Rule * Find out how the rules have changed and will continue to change * See the questions you are likely to be asked in a HIPAA Security compliance audit * Learn how to go about developing and implementing your  more...
Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel ...probably cannot afford to miss this important webinar! Areas Covered in the Session: * Why water myths develop o Impact of c-GMPs o Well-meaning but misguided precedents o Scientifically unchallenged traditions and benchmarking o Rule-hungry culture * Water System Microbial Control Myths o WFI from RO o Turbulent  more...
Electronic Raw Data in Regulated Environments - Definition Recording and Archiving - Webinar By GlobalCompliancePanel ...s * Checklist: FDA Record Retention and Retrieval Areas Covered in the Session: * FDA Requirements for raw data and meta data * FDA Inspection and enforcement practices * Recommendations from industry task forces: GAMP/ ISPE guides * Definition of raw data: original records vs. standard electronic formats, paper print-outs * Ensure and demonstrate integrity of  more...
Medical Device Reporting Regulations and Violations - Webinar By GlobalCompliancePanel ...Warning Letters to manufacturers for these violations. Areas Covered in the Session: * Review the FDA's Medical Device Reporting requirements. * Review FDA 483 MDR Reporting issues * Review Warning Letter Medical Device Reporting citations * Establish common problems in MDR reporting * What should MDR procedure contain? * What actions should be taken by  more...
Internal Audits Maintaining your Quality Systems at the Ready - Webinar By GlobalCompliancePanel Overview: While not captured in most audit reports, one of the biggest mistakes an organization can make is to have insufficient self audits. Internal audits are a core component of the Quality Assurance and Food Safety program. Ensuring the team representatives are trained and calibrated is a critical aspect of the program. An untrained team will miss important audit items, compromising the  more...
Operational Risk Management Ensuring Safety for Food Systems - Webinar By GlobalCompliancePanel ...ring the processes based on risk factors and ranking risk areas for purposes of preventive and corrective actions. Risk management requires no more or less management skill levels than any production, quality or purchasing operation - risk management simply requires attention. This session will establish a way of thinking about risks and their management that allows managers to simply define  more...
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Webinar By GlobalCompliancepanel ...es), Sponsors, and Institutional Review Boards (IRBs). Areas Covered In the Seminar: * Discuss how QA differs from QC and who is responsible for each * Determine who gets audited and factors and metrics for assessing when or why to audit * Discuss guidelines on how the FDA trains its investigators to audit Clinical Investigators (Sites), Sponsors, and Institutional Review  more...
Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel ...or the internal QA and external regulatory inspectors? Areas Covered in the Session: * Regulatory requirements for analytical instrument qualification * Calibration and Metrology Programs * USP * ICH Q2 * GXP * Equipment and Instruments - similarities and differences Who Will Benefit: This webinar will provide valuable assistance to all regulated companies  more...
Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ...tion and testing data and maintaining them in the DHR? Areas Covered in the Session: * FDA Quality Systems Regulation Requirements/ Definitions * MDD Requirements/ Definitions * Design History File (DHF) o Definition o Typical contents o DHF and outsourced design/ production o DHF and OEM relationships * Device Master Record  more...
New Changes to HIPAA The latest changes in the regulations and what they mean to you - Webinar By GlobalCompliancePanel ...viduals in the event of a breach are only two of the many areas affected in the new law, including new requirements for restricting and accounting of disclosures and increased enforcement activity. All kinds of covered entities, and now, business associates of covered entities and their subcontractors as well, need to review their HIPAA compliance, policies, and procedures to see of they are  more...
Excel Spreadsheets - Develop and Validate to Eliminate 483s - Webinar By GlobalCompliancePanel ...ke you a better Excel user, saving you time and costs. Areas Covered in the Session: * Become compliance when using Excel spreadsheets for GxP data. * Reduce validation time and costs. * Increase compliance while lowering resource needs. * Avoid 483s and Warning Letters. * Understand what validation documentation is required. * How to use Excel's audit trail.  more...
Understanding and Preparing for FDAs New Part 11 Inspection Program - Webinar By GlobalCompliancePanel ...nting Part 11 * Validation templates and examples Areas Covered In the Seminar: * FDA inspections: Preparation, conducts, follow up * Learning from past Part 11 inspections * Scope of the new Part 11 program: time frame, expected outcome * Criteria for selection of target companies * What inspectors are looking for * How to prepare your company for the  more...
Key Concepts in Successful Water System Sanitization - Webinar By GlobalCompliancePanel ... and troubleshoot the process for better optimization. Areas Covered in the Session: * Understand the basic water system sanitization concepts * Use this understanding to design effective microbial control measures for your water systems * Use this understanding to solve microbial problems originating from poor sanitization practices * Debunk a few water system myths  more...
Preventive and Corrective Maintenance Protect your assets Protect your consumers - Webinar By GlobalCompliancePanel Overview: A how to guide to meeting customer expectations of the maintenance function. An overview of industry best practices and a review of some leading software solutions. Why you should attend: Maintenance is often found to present the greatest area of opportunity for improvement in the food safety chain. Lack of control of parts and condition of equipment often contributes foreign  more...
Medical Device Tracking Latest FDA Update and Expectations - Webinar By GlobalCompliancePanel ...s will have different tracking methods and procedures. Areas Covered In the Session: * Review the key provisions in the updated FDA guidance on medical device tracking * Understand the regulatory expectations for device tracking * Identify new terms and criteria * Understand the statutory criteria and what changed * FDA has issued orders to manufacturers who are  more...
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant - Webinar By GlobalCompliancePane ...ticular site or even a study. Forewarned is forearmed. Areas Covered in the Session: * How to know when the protocol is not followed (PNF)? * What is the difference between a protocol deviation and a violation? * Importance of the "Protocol" in the number of deviations occurring * How to ensure that the protocol will be followed exactly? * What is in the Regs about  more...
Statistical Sampling Plans for Audits - Webinar By GlobalCompliancePanel ...on of different sampling strategies will be presented. Areas Covered in the Session: * Different types of sampling plans. * Measurement Error * Power Calculation * Types of Risk * Different Statistical distributions used for audit sampling Who Will Benefit: * Management * Research and Development * Regulatory Affairs personnel * Quality  more...
Recalls Removals and Market Corrections in Compliance with FDA and ISO Requirements - Webinar By GlobalCompliancePanel ... to result in the company's inability to ship product. Areas Covered in the Session: * Regulatory definitions of recalls, removals, and market corrections * Instances which require recalls, removals, or market corrections * What to do during recalls, removals, and market corrections * Recordkeeping requirements for recalls, removals, and market corrections * ISO  more...
FDA 483 Observations in the Laboratory What went wrong How can they be avoided - Webinar By GlobalCompliancePanel ...areas of concern to the FDA and other regulators, All units within each pharmaceutical firm should review recent regulatory observations and proactively establish programs or systems to address the regulatory concerns. In this webinar we will focus on the laboratory and recent FDA laboratory based operations. We will review observations, identify the real issue and suggest actions to prevent  more...
101 cGMP To-Do List for 2011 - Webinar By GlobalCompliancePanel ...ed into action in the past year will provide direction in areas of concern and what to expect in the future. This will be performed by a review of 101 areas of required review or industry problem areas. The result will be a basis for such a management review and a listing of likely milestones and tasks. Anticipation and addressing of weak spots proactively will further prove a company is "in  more...
A Comparison of ICH Q-10 Quality System and the FDAs Quality Systems Approach QSA to the Pharmaceutical GMPs - Webinar By Global ...ow to strike a balance between compliance and quality. Areas Covered In the Session: * What are the objectives of ICH-Q10 and the FDA's Quality Systems Approach to Pharmaceutical Good Manufacturing Practices? * What are the similarities and differences between these guidance documents? * What are some Pro and Cons of the product lifecycle for pharmaceuticals * Is the  more...
The FDAs Working Group Reports I II - New Directions - Webinar by GlobalCompliancePanel ...reports by the FDA's CDRH (devices) have identified major areas of concerns: 1) 510(k) Working Group's Preliminary Report and Recommendations, and 2) Task Force on the Utilization of Science in Regulatory Decision Making. Both Preliminary Reports and Recommendations were published August 2010, and stakeholders / industry is invited to comment. They recommend action on the part of both  more...
Basics of OTC Drug Labeling Compliance - Webinar By GlobalCompliancePanel ...ions regarding OTC drug labeling will also be covered. Areas Covered in the Session: * OTC Drug Labeling regulations: background and requirements * Drug Facts labeling * OTC Monographs and their importance * Conditions under which OTC Drugs can be marketed in the U. S.A. Who Will Benefit: Anyone who wants to market OTC drugs in the U. S.A. and assure that they're  more...
Introduction to Operational Risk - Webinar By GlobalCompliancePanel ...anking organizations to categorize and classify the major areas of operational risk. We will do a deeper dive into the two most critical elements of operational risk - legal risk, especially the risks from litigation and discovery, and the risks from financial crimes - internal fraud, external fraud, anti-money laundering, know your customer, etc. This three hour webinar is designed to provide  more...
Good Documentation Practices in a Regulated Environment - Webinar by GlobalCompliancePanel ...tical and medical device manufacturing, and their support areas. GDP describes the required activities and steps to use when recording data and other handwritten entries. Personnel, who work with documentation must be informed of these requirements, recognize their significance to their job and be aware of the consequences of non-compliance. During this 1-hour webinar, we will review the  more...
HIPAA Compliance and Workforce Training for Medical Practices - Webinar by GlobalCompliancePanel ...areas of the HIPAA regulations and their policy implementations at medical offices. The HIPAA Privacy Rule includes basic protections of uses and disclosures of protected health information that every staff member must be aware of, from avoiding discussion of patient-related information outside of the office, to taking precautions when faxing information to another office. Beyond the use and  more...
21 CFR Part 11 - Compliance for Electronic Records and Signatures - Webinar by GlobalCompliancePanel This webinar details the regulation and how it applies to computerized systems. Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach. This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to  more...
Auditing API Manufacturers and Suppliers - Webinar by GlobalCompliancePanel ...hat to examine, where to look, to whom to speak, and what areas are the best indicators of problems. Being able to find hidden signs of weakness or deviations that are not obvious are key to a good audit. Developing that talent and utilizing it are vital to the success of an audit and the auditor. Being able to discover "the smoking gun" is a key talent of a great auditor. It is always  more...
21 CFR Part 11 - What you need to know to pass the new FDA audits - Webinar by GlobalCompliancePanel This webinar details the regulation and how it applies to computerized systems. Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach. This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to  more...
How to Survive a DEA Audit or FINDFINE - Webinar by GlobalCompliancePanel This training entitled "How to Survive a DEA Audi or FIND=FINE" will cover all the record-keeping and security requirements that a DEA registered pharmacy must comply with when handling controlled substances and regulated chemicals. It covers all elements of what occurs during an unannounced DEA Diversion inspection and the auditing of all controlled substances and regulated chemicals. Why  more...
From The Elite Consulting Group, LLC
Marketing on A Budget on-line e-learning cbt (computer based)self directed This workshop has helped and will help you, the small business owner, work from home parent and entrepreneur. When markeitng we are all looking for affordability as well as an effective way to market. This seminar willgo over the different areas of marketing, how to find the cost effective way to market based on your company goals.  more...
From GlobalCompliancePanel
The DHF Technical File and Design Dossier - Similarities Differences and The Future - Webinar by GlobalCompliancePanel ...fering purposes / goals. Required and desirable contents. Areas requiring frequent re-evaluation / update. Similiarities and differences, and future trends. Typical DHF Table of Contents. Technical File or Design Dossier Table of Contents. The importance and usefulness of the "Essential Requirements". Structure of the "Declaration of Conformity"; self-declaring or N-B reviewed. Parallel  more...
Leadership in Manufacturing Contamination Control ...ertise. This broad manufacturing support role covers many areas, including routine raw material and product testing, disinfectant/ sanitant qualification, water and compressed gas testing, environmental monitoring, microbiological a awareness traininga of production operators, etc. Perhaps their most difficult leadership role is in contamination control investigations where product is at  more...
From McCord and Associates
Creating a Career Changing Personal Marketing Plan Workshop Series on-line e-learning cbt (computer based)workshop / seminartele-workshop series ...kes projections based on past history; identifies problem areas and sets out a detailed plan to correct them; establishes objective goals with specific timelines; and creates a monitoring methodology. This 6 week series of tele-workshops moves from an understanding of what a real marketing plan does, completely through the creation of detailed, career changing, workable personal marketing  more...
From Transient IT Solutions
ONLINE TIBCO TRAINING IN HYDERABAD ...enance across a range of vertical domains. Our main focus areas are: Banking, Healthcare Insurance, Telecommunications, Government, Manufacturing and Transporting. Trancient alliance partnership program is responsible for creating and developing relationships with leading and emerging technology companies. These relationships help us deliver the latest market leading research and innovative  more...
ONLINE JAVA TRAINING IN HYDERABAD on-line e-learning cbt (computer based) ...enance across a range of vertical domains. Our main focus areas are: Banking, Healthcare Insurance, Telecommunications, Government, Manufacturing and Transporting. Trancient alliance partnership program is responsible for creating and developing relationships with leading and emerging technology companies. These relationships help us deliver the latest market leading research and innovative  more...
From Fire Tech Productions, Inc
NICET Inspection Testing of Water Based Systems Level II CBT Webinar Series This webinar series covers all 3 areas of Level II exams, gives you 90 access, 24x7 to our online course modules, post tests and 3 simulated exams. The best NICEt prep around!  more...
From Coaches Plus
Coach Practitioner Course instructor led trainingon-line e-learning cbt (computer based)group study and discussionself directede-book ...on solid training and a clear sense of your strengths and areas for development as a coach * flexible requires tele-class/ web-conference attendance of half a day a week for 10 weeks so can fit around work/ life commitments * delivered through practical, interactive, teacher-led sessions, with lots of opportunity to practice and get feedback on your coaching * delivered by a  more...
From BMC Software, Inc
BMC Work Order Management 76 Using WBT Work Order Management is a back-end application of BMC Service Request Management (BMC SRM), providing basic facilities for assignment, status, work info, and task management. The SRM integration with Work Order Management allows users to create a generic work-order process. This online course provides Work Order Administrators and Managers with the information and experience they need to fulfill  more...
From TrainHr
Emergency Preparedness for Small to Midsized Companies - Webinar By TrainHR This webinar will highlight the basic areas which need to be addressed regarding the safety and security of your employees and your company. It will also cover topics for consideration in your Employee Policy Manuals, Safety Manuals, Procedural Manuals and Crisis Manual.  more...
From Business901
Marketing Your Black Belt Marketing Your Black Belt How Good are you at Marketing Yourself? Presentation on "How to Market Black Belt Services!" All Attendees will receive a Free download of How to Achieve Expert Status in 2010 Cana ™t make this time, please contact us for other available times. I believe that Lean Six Sigma Consulting has the greatest opportunity ever and in my terms,  more...
From CSS Computer Education
Computer Education Franchisee registered study center ...ch orientation has helped us continuously innovate in the areas of instructional design methodologies, and curricula development that is cutting-edge. The company provides a comprehensive education environment to individuals and enterprises, offerings training that is customized to the varied needs of audiences with diverse backgrounds. CSS Franchisee Network Programme has evolved over  more...
From Clinical Solutions Medical Training
OSHA Bloodborne Pathogens Certification Course ...am Goals and Objectives: 1. Identify when contaminated areas should be decontaminated 2. Discuss the transmission of Hepatitis B Virus (HBV) and importance of Vaccination 3. Explain proper disposal and handling of sharps 4. Explain the proper procedure for reporting exposure incidents 5. Identify personal protective equipment and its proper disposal 6. Discuss prevention techniques for  more...
From Scientific Bio-Minds
Diploma in Bio-Informatics instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewareworkshop / seminartrain the trainercomputer lab Scientific Bio-Minds is regarded as one of the leading bioinformatics institutions in India. Its Private organization mainly coordinates research and education in bioinformatics nationwide, and provides services to the life science communities that are highly appreciated worldwide. The Scientific Bio-Minds plays a central role in life science research both in India and abroad by developing  more...
From Global BioPharmaceutical Resources, Inc. (GBPR, Inc.)
21 CFR Part 11 the details of what it means This webinar takes the requirements of Part 11 and details them into specific things to do in all three primary areas: SOPs, product features, and validation. It describes what to do to be compliant thereby avoiding 483s and warning letters. All required IT SOPs are covered. All industry standards product features are discussed. The 10-step risk-based validation approach is outlined so that the  more...
Extractables and Leachables on-line e-learning cbt (computer based) As Single-Use Disposable Polymeric products have gained rapid acceptance by biopharmaceutical manufacturer worldwide, there are growing regulatory & industry concerns over leachables and extractables from these polymeric products. This webinar will review current standards and regulatory issues and discuss industry trends and developments. This webinar presentation will examine the key topics  more...
From TSN Technology
6 Months Industrial Training in Delhi for B TechBEMCA ...obal IT solution company providing full-cycle services in areas of Software Development, web design and development, web application development, professional ecommerce online shopping systems, Flash multimedia, website hosting, search engine promotion (SEO), portal development and graphics design. Combining our solid business domain experience, technical expertise, profound knowledge of latest  more...
From Online English Teacher
Online English Classes instructor led trainingon-line e-learning cbt (computer based)study at homegroup study and discussioncoursewareself directedcd rome-bookDVDbookworkshop / seminartrain the trainercomputer lab "Online English Classes" by Skype. Online English Teacher from England. Native English teacher from England, teaching English online since January 2007 - can teach for all different areas, such as IELTS, busines English etc. This is a proven effective method of teaching English - please get in touch if you are interested in learning like this. info@onlineenglishteacher. com http://www.  more...
From Consult SCM
SAP APO Supply Network Planning instructor led trainingon-line e-learning cbt (computer based) ...-APO (Supply Chain) via Web conferencing in the following areas: * SAP APO Demand Planning * SAP APO Supply Network Planning * SAP APO Production Planning and Detailed Scheduling * SAP APO Global Available to Promise * SAP APO Transportation Vehicle and Scheduling * SAP APO Supplier Network Collaboration Training is offered by experienced supply chain  more...
From Business Expert Webinars
Process Management for IT & Professional Services Firms ...r profit growth strategy. She teaches you to identify the areas of your business that are ripe for process management for both cost containment and reduction and the critical steps to implement the plan. Empowered with the knowledge from this eLearning event, you will be armed with the four-step system you need to create an efficient, scalable, metric-driven firm that can successfully compete.  more...
Process Management for Manufacturing & Construction Firms ...r profit growth strategy. She teaches you to identify the areas of your business that are ripe for process management for both cost containment and reduction and the critical steps to implement the plan. Empowered with the knowledge from this eLearning event, you will be armed with the 4-step system you need to create an efficient, scalable, metric-driven firm. In this webinar, you'll learn how  more...
Prosperity Economic Strategies for Business Executives ...uck Build focused momentum for exponential impact on all areas of your life As an added bonus, you'll receive Kim's prosperity checklist to help you implement her teachings. Kim Butler teaches Prosperity Economics nationwide to clients over the phone and web. She helps them implement strategies that get each of their dollars to do many jobs instead of only one job like typical financial plans  more...
Process Management for Manufacturing & Construction Firms ...r profit growth strategy. She teaches you to identify the areas of your business that are ripe for process management for both cost containment and reduction and the critical steps to implement the plan. Empowered with the knowledge from this eLearning event, you will be armed with the 4-step system you need to create an efficient, scalable, metric-driven firm. In this webinar, you'll learn how  more...
Survive and Thrive In Economic Turbulence ... productivity to find energy leaks, financial drains, and areas to prioritize for improvement. Learn to draw out the highest contribution from your staff members Understand what creates a lean, high-performance team..and the fastest way to whip your team into shape. Begin to define a new paradigm for these more turbulent times Rhoberta Shaler, PhD, is a woman on the move with a  more...
Prosperity Economic Strategies for Business Executives ...ck Build focused momentum for exponential impact on all areas of your life As an added bonus, you'll receive Kim's prosperity checklist to help you implement her teachings. Kim Butler teaches Prosperity Economics nationwide to clients over the phone and web. She helps them implement strategies that get each of their dollars to do many jobs instead of only one job like typical financial plans  more...
Success Strategies for Small Business Owners ...his webinar, you'll learn how to: Identify the right areas of your business to measure and use those metrics to drive change Solicit information from others for intelligent decision-making Use positive selfishness when making decisions on your time and resource investment Feel confident saying, 'No!' to business distracters that are outside of your focal area As an added  more...
Brand Busters: How What You Say And Do Can Ruin Your Reputation ...rld examples, you ll discover: The three critical areas where your customers are evaluating you The difference between brand identity and brand behavior Where 'brand leaks' typically occur Why to use a script and what can happen if you don t The importance of consistency and how to get others on board Sarah Day is a business advisor who helps the owners of small to  more...
Keys to Unlocking Your Employees Potential ...arn to: Identify and prioritize employee development areas Uncover your employees strengths and how to apply them to their existing responsibilities Overcome your natural discomfort discussing performance issues Motivate employees so they can learn to take charge of their own performance Conduct effective employee meetings that leave them pumped with enthusiasm As an  more...
Process Management for Manufacturing & Construction Firms ...r profit growth strategy. She teaches you to identify the areas of your business that are ripe for process management for both cost containment and reduction and the critical steps to implement the plan. Empowered with the knowledge from this eLearning event, you will be armed with the 4-step system you need to create an efficient, scalable, metric-driven firm. In this webinar, you'll learn how  more...
Business Development Secrets for Consultants ...wareness without emptying your wallet High impact growth areas to leverage in a slow economy for rapid business development As an added bonus, you will receive Dr. Drew's whitepaper 'Business Building Techniques' to help you implement his teachings in your consulting practice. Drew Stevens PhD, President of Stevens Consulting Group and renowned author, consultant and sales expert literally  more...
Prosperity Economic Strategies for Business Executives ...uck Build focused momentum for exponential impact on all areas of your life As an added bonus, you'll receive Kim's prosperity checklist to help you implement her teachings. Kim Butler teaches Prosperity Economics nationwide to clients over the phone and web. She helps them implement strategies that get each of their dollars to do many jobs instead of only one job like typical financial  more...
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