Each Web-based Seminars

ITIL v3 Service Transition Lifecycle Course This 3-day course immerses learners in the overall concepts, processes, policies and methods associated with the Service Transition phase of the Service Lifecycle. The course covers the management and control of the activities and techniques within the Service Transition stage, but not the detail of each of the supporting processes. This course is designed using an engaging scenario-based approach  more...

Health Information Technology Introduction ...cation courses at their local college and/ or university. Each of the sessions below are three to four hours long. These sessions along with certification from an approved certification center will prepare you for a career in Health Information Technology. HCMI Solutions Internship opportunities are available upon completion of the sessions below and registration in an approved Health  more...

Health Information Technology Systems ...cation courses at their local college and/ or university. Each of the sessions below are three to four hours long. These sessions along with certification from an approved certification center will prepare you for a career in Health Information Technology. HCMI Solutions Internship opportunities are available upon completion of the sessions below and registration in an approved Health  more...

DISC Training Webinar DISC TRAINING | Friday, February 24, 2012 | 1: 00 PM a 3: 00 PM CST Led by Paula Fracasso Discover your own behavior and how to relate best with each behavior style. Go beyond the interview and learn to accurately use the DISC Assessment tool when hiring. Learn to effectively coach your employees and/ or understand how to best train and manage an employee. **Tuition is $99 (includes cost  more...

Data Mining for CRM using STATISTICA Data Miner This course introduces you to the area of customer relationship management (CRM) and the STATISTICA Data Mining10. 0 interface. You are introduced to the different learning methods of parametric statistical analysis and data mining analysis, and introduced to the practice of combining several modeling algorithms (ensembles) to predict customer responses. The methodological emphasis of this course  more...

Accelerated PMP E Learning ...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 your doubts. Question bank of 1500 questions covering all the knowledge areas & processes. Audio recordings of faculty available for repeated listening, thus facilitating self paced learning. Contents for  more...

Live Online Course for gaining PDUs Towards the advancement of Project Management knowledge, after acquiring PMP Certification you require continuing the certificate (CCR).Certificate is valid for 3 years & 60 professional development units (PDUs) are required during each three-year certification/ CCR cycle. PMSoft provides facility to earn PDUs through Free Live, Online PDU Sessions on various topics related to Project,  more...

Navigating the Alphabet Soup of Employment Law - What Every Manager Needs to Know ...USERRA. Learn how to avoid Employment Law liability under each of these statutes. Find out how each of these laws interacts with the others to ensure that your company is in full Employment Law compliance and adequately protected. Learn how to protect your company and yourself (managers can be held personally liable under most state fair Employment Laws, for example under New York Statea  more...

Cancer in the Workplace - Best Practices and Tips for HR There is no doubt that medical issues and requests for leave of absence are a common nightmare for HR. Moreover, recent statistics suggest that cancer is one of the most debilitating illnesses that workers have. Yet many employees are able to continue working while receiving treatment. According to the EEOC, more than one million Americans are diagnosed with some form of cancer each year and  more...

MULTI-STATE EMPLOYERS TIPS FOR DRAFTING EMPLOYEE HANDBOOKS FOR ALL LOCATIONS Multi-state employers face many legal pitfalls when drafting their employee handbooks. Learn how to avoid these legal perils and ensure compliance with the state laws of the states in which you operate. This on-line interactive webinar will help you understand how to treat each state's legal requirements when drafting your employee handbook.  more...

SUBSTANCE ABUSE AND THE ADA WHAT YOUR MANAGERS NEED TO KNOW ...lics and Drug Addicts also can cause issues. Find out how each of these is treated by the ADA and get best tips on how your managers can best manage these employees and still be legally compliant. In this 60 minute webinar presented by attorney Melissa Fleischer, you will learn: a Tips to keep in mind when handling workplace substance abuse issues a Misconceptions that may lead to  more...

From Hiring To Firing What Every Manager Needs to Know ...ADEA, GINA and USERRA. Learn how to avoid liability under each of these statutes. Find out how each of these laws interacts with the others to ensure that your company is in full compliance and adequately protected. Most employers do not know that in many states the state employment discrimination laws apply to employers with small numbers of employees such as 4 or more employees. In addition,  more...

Listening for Tech Entrepreneurs Tech Entrepreneurs can be so steeped in their product that they don't pay attention to what is happening around them, then they wonder why they're not getting funding, a market, or customers. A major factor in this challenge is the lack of well developed listening skills. Many tech entrepreneurs have no idea how they listen, let alone if their listening habits are appropriate for the situation  more...

Tune Up Your Listening ...each 90 minutes webinar #1 builds awareness of listening habits and their impact on communication. Participants take the assessment instrument, Hear! Hear? Your Listening Portfolio that describes their use of four different listening habits. Participants examine how they prefer to listen, their listening strengths and challenges, and the appropriateness of their listening habits at work.  more...

SOA BPEL Online Training ...standard protocols like WSDL, HTTP etc. The idea is that each of the applications expose themselves as services that can talk the same language. And then we have a 'glue' that binds all these services together. Essential to successfully utilize SOA is mastering the technologies (the 'glue') that are used to develop SOA applications - BPEL and ESB. In this course, we learn both of them.  more...

Introduction to Visual Basic for Applications (VBA) In this introductory Visual Basic for Applications (VBA) training course, you will learn how to manipulate objects in Word, Access and Excel with VBA. Specifically, you will learn how to use the Visual Basic editor, work with the object model, create and use variables, and use the selection structure.Each lesson of the class begins with a general overview of a feature and then shows how that  more...

Advanced Visual Basic for Applications (VBA) In this advanced Visual Basic for Applications (VBA) training course, you will learn more advanced features of VBA. Specifically, you will learn to use flow control, work with the Office Assistant, create custom dialogs, automate processes and handle errors. Each lesson begins with a general overview of a feature and then shows how that feature works in each of the Office applications.  more...

Object-Oriented Analysis and Design (OOAD) Training with UML ...ated Analysis and Design (OOAD) with UML training course teaches students how to use object-oriented techniques from requirements gathering to implementation. Learn how to analyze and design classes and their relationships to each other in order to build a model of the business requirements. All the UML diagrams are covered in this OOAD class to identify the most suitable diagram suite for your  more...

Oracle Database 10g: Administration Level II ...ailure scenarios and the best recovery strategies for each. Strategies for on-line backups, complete and incomplete recovery, media recovery vs. flashback database recovery and many other subjects are discussed. Extensive exercises allow students to simulate failures and perform actual recovery within the workshop. Additionally, some of the most exciting new technologies  more...

Introduction to EJB 3.0 This course introduces the experienced Java developer to Enterprise JavaBeans -- the Java EE standard for scalable, secure, and transactional Java components. EJB 3.0 has reinvigorated this area of Java enterprise development, with dramatic improvements in ease of use and smooth integration with servlet-based or JSF web applications. This course treats the 3.0 specification, with a few notes on  more...

Comprehensive JSP Training ...ess and transform XML data using XPath and XSLT. Each individual tag in each library is covered, with precise syntactic rules shown in a standard format in the student guide, and JSTL techniques and best practices are discussed for each library. An extensive set of example applications illustrates common usage of each major group of actions, and the module culminates with a wrap-up  more...

Java EE Seminar for Managers This course provides a coherent, high-level explanation of the Java Platform, Enterprise Edition (Java EE): what sorts of software are created with Java EE; how software is developed for this platform; how it is deployed and put into production; how it can be administered. The course is designed specifically for non-programmers -- analysts, managers, technical writers, and anyone who desires a  more...

Java Swing Training ...werful controls are studied: the tree and table controls. Each is presented in a separate chapter, allowing students to dig into the underlying architecture and to develop a firm grasp of the many powerful features lying behind the direct use of the control classes themselves. Especially, customization of the controls using renderers and editors is considered. The final chapter of this module  more...

SharePoint 2007 Governance Training This SharePoint training course covers the ins and outs of governance in general as well as common taxonomies. You will review what a Governance plan is made up of, as well as learn how to create a training plan, SharePoint service offerings and how to follow through with enforcing the plans. We will review Information Architecture and why it is important.We will take a look at each level in  more...

Advanced Adobe Captivate 4 Training In this advanced Captivate training class, you will learn Captivate ' s higher-end functionality while improving your production skills via project templates, design templates, advanced actions and scripts. You will learn to collaborate with team members via Captivates ' powerful commenting features. You ' ll enhance your users experience via variables that will make it seem like each eLearning  more...

Change Management Training ...eaches students how to develop the skills to proactively address change and meet the challenges of transition in the workplace. Students will work with various employees to overcome the problems encountered when making changes in your organization. Students will also learn how to develop the ability to effectively handle organizational changes by examining the transition process and  more...

Six Strategies to Grow Aggressively in the Federal Market webinar on June 14th 2012 ...arly bird registration pricing a it ends 3 weeks before each class. Register at www. ostglobalsolutions. com/ training/ schedule Date, 2012 Class Name June 19-20 Advanced Capture Management June 21-22 Advanced Proposal Management July 19 Proposal Win Themes Development Workshop July 20 Executive Summaries For Winning Proposals Workshop If you don't find a class that suits your schedule,  more...

Implementing Statistical process Control SPC for Short Run Production ... happens when you run a variety of small production lots, each with different dimensions, nominal values, material properties and dimensional tolerances? How can you derive a statistically significant sample that will allow confidence in the final measurements and interpretation of those measurements? The answer is found in a little-taught variation of SPC technologya Short-Run SPC.  more...

Understanding Improving Yields Scrap Rework ... and rework. The proper use of these terms as well as how each is calculated and monitored will be demonstrated. Specifically, we will address: - How to PROPERLY measure yieldsa why is a yielda different from scrap? - How to PROPERLY measure and account for scrapa what does scrap REALLY cost? - Why yield and scrap metrics should NEVER be confused. - How to segment and  more...

The Most Important Metrics For Measuring Supply Chain Performance .... The a Modem Chat Seriesa Webinar leader will explain each of these common metrics and demonstrate how each is calculated. Participants will be encouraged to share their ideas and views in this fully interactive LIVE web conference format. Participants should be prepared to openly discuss their ideas and to interactively comment on other participanta ™s ideas presented during this LIVE  more...

How to Conduct an Effective Monthly Variance Review Meeting ...rs always conduct a routine a Variance Review Meetinga each month, challenging their direct reports to explain all significant variances from plan. These variances are usually, though not always, stated in terms of dollars. Specific variance that great plant managers have a tendency to routinely review, include: + Closed Order Variances + Purchase Price Variances (PPV) + Burden  more...

Constructing a Component Criticality Matrix A Better Way to Identify Important Components ... parts and Suppliers makes it nearly impossible to manage each individual part as much as one wants to. This is why Procurement organizations rely upon stratification methods and other sorting methodologies to provide insights into GROUPS of parts. This way, the Purchasing professionals can focus on the important few parts while not wasting time on the trivial many parts. The Component  more...

Demystifying the Calculations of Efficiency Utilization and Productivity ...he common language we use in business to communicate with each other breaks down. So it is with the manufacturing industrya ™s standard terms; efficiency, utilization and productivity. These terms, though each having distinctly different meanings with distinctly different consequences, are often incorrectly interchanged especialy efficiency and productivity. This 1-hour FREE webinar  more...

Operations Improvements Monthly Webinar each month on the 3rd Thursday, this Webinar series addresses one or more SPECIFIC issues facing OPERATIONS professionals in the maufacturing and distribution industries.  more...

Become an Email Genius Email Etiquette and Writing Tips that Get Your Emails Noticed for the Right Reasons ...llions of dollars are wasted, along with countless hours, each year in email misuse. Learn what it takes to create effective emails. Agenda: Learn how email has affected the way we communicate today What readers demand if they are going to read yours How to reduce email writing time by one third the time The importance of subject lines and how to write them Dealing with strings of emails  more...

RAPS Approved Seminar on Complying with GMP and CGMP Requirements Streamlining Quality Assurance and FDA Compliance at Mumbai ...Each lecture will be 90 min in length. There will be morning and afternoon breaks of 30 min each which will be reduced to 15 min, if needed to accommodate long lectures. Lunch will be at least 1 hr in length. The instructor will be available for questions and discussions during all breaks and lunches and will also be available for a minimum of 30 min at the end of each day. The first daya  more...

What to do if you get a FDA 483 Warning Letter - Webinar By GlobalCompliancePanel Overview: Audits by the FDA are perhaps the most intimidating of all events at a regulated facility. Each year, the FDA conducts several thousand audits, approximately half of which lead to findings that result in Form 483s. Thursday, March 29, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

Effective Hazard Analysis to Meet FDA and ISO 13485 2003 Risk Management Requirements - Webinar By GlobalCompliancePanel Overview: FDA-GMPs, known as Quality System Regulations (QSRs), and ISO 13485 require Risk Management as integral part of the development life cycle. The starting point for each risk management lifecycle is the Hazard and Risk Analysis which provides safety critical design input for the device design. Price List: Live : $245. 00 Corporate live : $995. 00 Recorded : $295. 00  more...

Interfacing Design Verification Process Validation and Design Validation - Webinar GlobalCompliancePanel Overview: There is confusion between the requirements for Design Verification, Process Validation and Design Validation. While each of these processes has its own requirements, they do not stand alone, they are linked together. As this linkage is not well understood, it is the source of FDA observations and potential release of products that do not meet requirements. Tuesday, March 13, 2012  more...

Management Styles that Work Best for Each of the Four Generations in the Workplace - Webinar By TrainHR This session is designed to help you manage more effectively by being able to differentiate between each generation and adapt to their style and outlook and capitalize on their strengths  more...

Portfolio Optimization for Global Drug Development - Webinar By GlobalCompliancePanel Strategic portfolio planning is crucial for developing long-term company strategy. The goal is to meet strategic objectives selecting the "best" portfolio of internal and external drug development programs for funding and balance company resources including money, manpower and manufacturing capacity. Projects could be interdependent, have multiple development scenarios, and are subject to multiple  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...

Hybrid Quality Systems For Pharmaceuticals - Combining ICH Q7A Part 210-211 - Webinar By GlobalCompliancePanel The manufacture of drugs is controlled by ICH-Q7A and 21 CFR Part 210 & 211. Although these standards were written 24 years apart, they complement each other in many ways. Thursday, September 29, 2011 10: 00 AM PDT | 01: 00 PM EDT  more...

Introduction to Contamination Control Master Plans - By GlobalCompliancePanel ...inants. However, due to variable emphasis being placed on each of these control elements by FDA auditors, most manufacturers have developed their programs in a piecemeal fashion. Thus, each element in a manufacturer's control program has been implemented without regard for the effect of the other elements. As a result, potential complimentary synergies between control elements have typically  more...

Calibration Concepts for Auditors and Reviewers - Webinar By GlobalCompliancePanel This presentation will provide an overview of the rules and assumptions behind the calibration of analytical instruments. We will discuss how external standard, internal standard, and isotope dilution methods are designed, and learn the situations where each technique is the best option.  more...

Excel Spreadsheet Validation to Eliminate 483 - Webinar By GlobalCompliancePanel This interactive webinar provides explicit details and live demonstration followed by a collaborative workshop that explains how to configure and validate a GxP compliant spreadsheet application. What makes this session unique is the combination of step-by-step instructions and the hands on workings of each participant. Bring your laptop and use Excel for yo  more...

SAP FICO Online Competency Development Training program ...rials: All attendees would receive a Assignment after each module, a Notes and study material for examples covered. a Access to the Training Blog Training Format: This course is delivered Online using Web and Audio Conferencing. Timing: Weekdays and Weekends after work hours. ABOUT THE TRAINER: a More than 8 years of Consulting & Teaching experience in different modules  more...

JAVA J2EE JEE Professional Role Based Training from Zaran Tech ...rials: All attendees would receive a Assignment after each module, a Notes and study material for examples covered. Training Format: This course is delivered as a highly interactive session, with extensive live examples. This course is delivered in Online using Web and Audio Conferencing. Timing: Weekdays and Weekends after work hours. ABOUT THE TRAINER: 1. Worked in various  more...

SAP BOBJ with BW integration Online Competency Development Training program ...rials: All attendees would receive a Assignment after each module, a Notes and study material for examples covered. Training Format: This course is delivered as a highly interactive session, with extensive live examples. This course is delivered in Online using Web and Audio Conferencing. Timing: Weekdays and Weekends after work hours. ABOUT THE TRAINER: a More than 12 years  more...

Business Analyst Competency Development Program ... documents, Training materials for our training program, (each video is less than 5 min long but gives you a good idea about our training to placement process) During the Training: Video 1 a Explains what our training program consists of Video 2 a What happens after you Signup? - Video 3 - During the Training Process - Video 4 a How we use Googledocs to share documents/ materials  more...

Device Master Record Device History Record BY GCP The FDA's Quality System Regulation (QSR) requires each device manufacturer to compile the specifications and procedures for a medical device.  more...

The Law and Psychology of Mental Health Issues at Work Substance Abuse Depression and the Bermuda Triangle of the ADA the FMLA a ...em get help, this 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  more...

The 510k Submission Requirements Contents and Options - Webinar by GlobalCompliancePanel Overview: This presentation will provide an understanding of how to get a device requiring a 510(k) submission to market quickly. Knowing when and how to properly submit a 510(k) for a device or change to a device is critical to a company's regulatory and financial health. Your goal is to get the 510(k) through the review process as quickly as possible. This presentation will also distinguish  more...

Product Recalls - Planning and Conducting Food Recall - Webinar By GlobalCompliancePanel Creating an effective Product recall process that will protect both the consumer and company's/ brand's reputation requires careful planning and active involvement of each involved department.  more...

Instructor-Led Live Online Video Training - leadership classes Instructor-Led Live Online Video Training a Near Classroom Superior Experience Instructor-Led Live Online Video leadership classes How Does the OnLine Program Work? The Instructor-Led Live Online Video leadership classes are conducted in real time, by a live instructor in a remote location and a number of employees in their own worksite. The employees may be located in their companya  more...

Information Security Risk Analysis Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePane ...e assessed for risks. Risk issues and recommendations for each system or information flow can then be described and organized into a table that is used to define the risks and prioritize their mitigation, using a straightforward high-medium-low stratification of potential likelihood and impact for each risk issue, following the risk determination method identified in the preamble to the HIPAA  more...

Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel ...PA definition * the CAPA LIFE cycle * Tools for each CAPA cycle * CAPA requirements * Tools for Preventive Action * Common FDA CAPA findings and how to avoid them Areas Covered In the Session: * Off-label statute * Label claims * Allowable reprints * Promotional compliance * FDCA: The law Who will benefit: * Sales executives in  more...

21 CFR Part 11 How to Successfully Prepare for and Host an FDA Inspection - Webinar By GlobalCompliancePanel ...on, electronic records will be more needed and desired in each organization. In addition, approval of documents and records in a timely fashion is absolutely needed at all times, and being able to do just that via an electronic media is understood. For both, electronic signatures and electronic records, the organization shall comply with the Part 11 regulation. Areas Covered in the Session:  more...

Gowning Systems Used in Cleanrooms Controlled Environments - Webinar By GlobalCompliancePanel ...gowning techniques and sequence. * Discuss what role each garment part plays in contamination control and human safety. * Explore expectations of cleanroom garment suppliers. * Discuss cleanroom gowning tests and personnel qualification. Who Will Benefit: * Q Auditors and Personnel * Manufacturing Operators * Maintenance and Cleaning Personnel *  more...

Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel ...C * Qualification and documentation requirements for each category * Going through the category example list * Approach for existing systems * Approach for automated systems (incl. firmware/ computer systems) * Requalification after equipment changes (move, repair, firmware upgrade, hardware upgrade) * Documentation requirements Who Will Benefit: * QA  more...

HIPAA Breach Notification What to do to prevent breaches and what to do when they happen to you - Webinar By GCPanel ...each Notification Rule required by the HITECH Act within the American Recovery and Reinvestment Act of 2009 went into effect September 23, 2009, requiring all HIPAA covered entities and business associates to follow a number of steps to be in compliance. * The HIPAA Breach Notification Rule has been in effect since September 23, 2009 and most organizations are not prepared to respond to  more...

Excel Spreadsheets Step-By-Step Instructions for Compliance - Webinar By GlobalCompliancePanel ...of step-by-step instructions and the hands on workings of each participant. Bring your laptop and use Excel for your own needs. This session will make 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  more...

The Investigation System Discovery Planning Root Cause Analysis CAPA - Webinar By GlobalCompliancePanel ...fective and efficient investigations. Topics will examine each step of the investigation process from failure identification and notification through documentation. Participants will review root cause analysis techniques and observe how to identify corrective and/ or preventive actions towards successful remediation and closeout. This high-level overview will provide clarification on the steps  more...

Recruiting is Critical to Your Success What is the Secret - Webinar By GlobalCompliancePanel ...or steps in the recruitment process and the importance of each Who Will Benefit: This Webinar will provide invaluable assistance to investigators and their staff in the regulatory / legal responsibilities and also the ethical considerations in pharmaceutical product (Drug or device) research involving human subjects. Those benefiting the most would be: * Principal Investigators and  more...

Understanding the Calibration Curve - Webinar By GlobalCompliancePanel ...tion methods are designed, and learn the situations where each technique is the best option. Whether you use single point calibration, or linear regression, we will discuss the strengths and weaknesses of each approach. If you must generate and evaluate calibration "curves" we will show you why the correlation coefficient is only one option for the evaluation, and why sometimes it can give a  more...

Design Control for Medical Devices - Webinar By GlobalCompliancePanel ...s already in distribution. Documentation requirements for each design stage will be included as well. Why you should attend: Because design controls must apply to a wide variety of devices, the regulation does not prescribe the practices that must be used. You need to be aware of how design control applies to your device(s). It's apparent many firms are not: inadequacy of the design control  more...

How to use QSIT to Your Advantage - Webinar By GlobalCompliancePanel ...o enable them to prepare for the inspection. Delving into each and every section of the QSIT, this webinar also includes straightforward, helpful methods for incorporating it into your companya ™s ongoing quality system. Why you should attend: If you don't know what the FDA inspector is going to look at when (s)he performs his/ her audit, how can you really know what to prepare for?  more...

Best practices for conducting OOS investigations - Webinar By GlobalCompliancePanel ...rformed. Common pitfalls and means of overcoming them at each of the steps will be identified by a review of recent Warning Letters. The structure of an Investigation report which satisfactorily documents the investigation will be discussed. Ample time will be available for Q&A halfway through the webinar and at the end. Why you should attend: FDA inspectors have in the past identified OOS  more...

Introduction to Contamination Control Master Plans - Webinar by GlobalCompliancePanel ...inants. However, due to variable emphasis being placed on each of these control elements by FDA auditors, most manufacturers have developed their programs in a piecemeal fashion. Thus, each element in a manufacturer's control program has been implemented without regard for the effect of the other elements. As a result, potential complimentary synergies between control elements have typically  more...

Effective Corrective and Preventive Actions CAPA 10 Steps to Success - GlobalCompliancePanel Virtual Seminar - Webinar By Global ... Supporting stories and practical examples of CAPA - when each is appropriate and when one or the other is not appropriate + The regulations and international requirements for CAPA and the clear understanding how to suit your procedures, work instructions and forms to address it * Module 2 o Examples of problem solving tools, management tools and measurement  more...

Hazard Analysis vs FMECA Differences and Commonalities - Webinar By GlobalCompliancePanel ... will show ways how these tools can be used to complement each other. Additionally the differences and limitations of both methods will be illustrated and the appropriateness during the different product development phases will be discussed. Areas Covered in the Session: * Hazard analysis techniques * FMECA techniques * Probabilistic approaches * When to use which  more...

Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel ...obial control approaches as well as microbial monitoring. Each myth will be explained as to its origin and then put into true context with how the supposed microbial control or monitoring approach SHOULD be handled. You will probably be surprised to learn which of your "rules of thumb" are actually quite wrong! Perhaps you will find out why you are having microbial problems in spite of using  more...

Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Webinar By GlobalCompliancepanel ...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 Boards (IRBs) * Review recent noncompliance trends and regulatory focus for Sites, Sponsors,  more...

Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel ...ated. This seminar will review the regulations that cover each environment and present simple and effective strategies for satisfying the requirements. The impact of USP on analytical instrument qualification will be reviewed and the newest regulation will be presented in a simple and understandable way. The interaction of calibration, qualification, method validation and equipment maintenance  more...

Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel ...oks at these principles and the processes associated with each principal to design, implement, and maintain a combination system that surpasses compliance requirements. The seminar will focus primarily on the principles embodied in CFR Parts 210-211 and ICH Q7A for pharmaceuticals and Part 820 for medical devices as well as pertinent passages of the International Conference on Harmonization  more...

Excel Spreadsheets - Develop and Validate to Eliminate 483s - Webinar By GlobalCompliancePanel ...of step-by-step instructions and the hands on workings of each participant. Bring your laptop and use Excel for your own needs. This session will make 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  more...

FDA 483 Observations in the Laboratory What went wrong How can they be avoided - Webinar By GlobalCompliancePanel ...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 similar  more...

101 cGMP To-Do List for 2011 - Webinar By GlobalCompliancePanel ...and in any remediation efforts. Why should you attend: Each year companies are to perform a complete review of their quality management system and its ability to meet the current GMP's. To add to the urgency, there has been a major shift in the emphasis of the U. S. FDA cGMP compliance audits, clinical trial expectations, product submissions and company response requirements. In short, all  more...

The Advantages of Linking Management Systems - Webinar by GlobalCompliancePanel Overview: It's important to improve the dialogue between financial, quality, IT and environmental management systems. Members of these management systems need to understand what the others do. Quality and environmental managers need to understand the language of finance and the effect of operations on the bottom line, while financial managers need to know how quality, environmental and IT  more...

The Drug Development Path - From RD to Commercialization - Webinar By GlobalCompliancePanel ... drug development process, reviewing key deliverables for each stage of the development path with a special focus on managing the development process when using external resources such as Contract Manufactures, Contract Testing Labs and Contract Research Organizations. In today's fast-paced, highly regulated and risk-aversive environment, functional groups can no longer work in isolation,  more...

Full Day Virtual Seminar - Designing and Implementing the Quality System for Combination Products - by GlobalCompliancePanel The FDA generally defines combination products as a product composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device, and a biological product. Although there are differences between these quality systems, the quality principles embodied in the systems are the same. This course looks at these principles and the  more...

Interfacing Design Verification Process Validation and Design Validation - Webinar by GlobalCompliancePanel There is confusion between the requirements for Design Verification, Process Validation and Design Validation. While each of these processes has its own requirements, they do not stand alone, they are linked together. As this linkage is not well understood, it is the source of FDA observations and potential release of products that do not meet requirements.  more...

BRC Risk Analysis - Webinar by GlobalCompliancePanel Risk Assessment is a fundamental and intuitive activity that is not new to manufacturing professionals. Bringing consciousness and tangibility to this process is the challenge often faced. A practical guide documenting the process will be the topic of this training. This presentation will take you step by step through the creation of each type of risk assessment required by the BRC. Process and  more...

Statistical Concepts of Process Validation - Webinar by GlobalCompliancePanel The FDA QSR requires device manufacturers to validate processes when the manufacturer cannot "fully verify the output". The manufacturer must validate these processes with a "high degree of assurance". The presentation explores the statistical underpinnings of these two phrases. To "fully verify the output" relates to the use of statistical sampling plans, while "high degree of precision"  more...

Excel Spreadsheet Validation To Eliminate 483s - Webinar by GlobalCompliancePanel This interactive webinar provides explicit details and live demonstration followed by a collaborative workshop that explains how to configure and validate a GxP compliant spreadsheet application. What makes this session unique is the combination of step-by-step instructions and the hands on workings of each participant. Bring your laptop and use Excel for your own needs. This session will make  more...

The FDA Tripod - Clinical Trial Regulations Compliance and GCP in Drug Development - Webinar by GlobalCompliancePanel This course provides a comprehensive review of Good Clinical Practice (GCP) and FDA regulations and requirements. Participants receive a foundation of knowledge about GCP, practical examples, and the underlying scientific and regulatory principles involved. Guidelines for each aspect of research are provided, as well as information on the structuring and preparation of protocols, consent forms,  more...

Auditing a Process-based System - Compliance Training Seminar by GlobalCompliancePanel There are a number of reasons for someone to attend this webinar. First and foremost they will gain an understanding of the process approach. The process approach requires management to identify all processes of the QMS, their sequence and interaction. They must ensure the effectiveness of all processes and the availability of needed resources, and monitor, measure, analyze and improve them. They  more...

PCI Data Breaches What happened What may have prevented it What if it happens to you ... go after whatever is easy. The cost of responding to a breach is getting more expensive each year. In this webinar you will learn about the current threat environment, how some of the biggest data breaches of recent years could have been prevented, how to reduce your risk of a breach and what to do if the unthinkable happens. Compliance with the PCI DSS is expensive, no argument there.  more...

Online Building Science Series March - August 2010 If you are interested in learning about the fundamentals of building science and the energy efficiency industry, or becoming a certified Energy Auditor, this series of online courses is for you. Every other week starting in March 2010, our online series will support you in becoming a building performance professional from the comfort of your home or office. Each interactive course is presented in  more...

Adobe eLearning Suite ...plementing digital media tools into a workflow. Before each on-site training session, we take a close look at your current production process, software, resource skill sets, and types of Adobe eLearning Suite content being created. From this data we can distill a training program that not only meets your current needs, but also provides a path for the future. Call today to schedule an  more...

online pgmp workshop Weekend online workshop to prepare candidates for PgMP Exam Certification. This workshop will help leadership and senior management team to achieve dual purpose. 1. Preparing for PgMP Certificate 2. Enable them to create the Program in real world. These skills will empower participants to grow next level of project management in the professional career by adding value to their organization  more...

Excel at Filing - On-Demand Webinar The computer is an excellent organizing tool and yet the last thing clients want to do is buy more software. In this popular webinar, Certified Professional Organizer ® Debra Milne takes you through the different ways Microsoft Excel ® can be used to create an electronic filing system including electronic filing practices; printing file inventory lists; searching and tracking files;  more...

Creating a Career Changing Personal Marketing Plan Workshop Series ...attacked and marketing methods that will be used; creates each marketing piece; identifies exact past history production percentages and ratios; makes 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  more...

Improving Communication ... of communication that are effective and ineffective with each style Develop specific communication strategies that build a culture of alliance and collaboration You can register for this class online, within 24 hours you will receive an e-mail with a link with instructions, please follow the link and directions, when answering the questions on the questionnaire - think of your  more...