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Grow Spiritually Succeed Managerially Thinking is an art, a skill and one needs to practice it like a musical instrument or a sport. A successful manager or a leader must learn how to use this wondrous equipment in order to think, to reason and decide his / her course of action(s) in personal as well as professional life. Learning Objectives: History of human development, Intellect Vs Intelligence, Objectivity at work, 3 C's of  more...

Introduction to Visual Basic 2008 Training ...Basic 2008 language features that you must internalize in order to create full-featured Web or Windows applications that make best use of the .NET 3.5 platform.You will learn about data types, variables, and operators, along with all the important flow control structures. You ' ll work through several examples demonstrating the power of the .NET 3.5 Framework, and dig into creating and  more...

Object-Oriented Analysis and Design (OOAD) Training with UML ...d 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 organization. An emphasis is placed on Use Cases to capture and manage requirements and form the basis for test scenarios. Class relationships, through the use of Design Patterns,  more...

MOC 8822 - Purchase Order Processing in Microsoft Dynamics GP 10.0 This Microsoft Dynamics GP class will help students prepare for the following Microsoft Certified Professional exam: Exam GP 10.0 Inventory and Order Processing.  more...

MOC 8824 - Sales Order Processing in Microsoft Dynamics GP 10.0 ...Order Processing class explores the accounting cycle and the processes required to enter and ship sales orders. This class shows you how to easily manage the life-cycle of your customer ' s order from the initial quote to the shipment documentation and final invoicing. You learn how to perform additional functions setting up process holds for quality assurance and linking order documents to  more...

Introduction to Java Training This Java training course is intended for students without an extensive programming background. It covers most Java syntax elements, concentrating on fundamental and universally useful elements, while providing an overview of many more advanced elements. Students will learn to write useful Java classes, applying Object-Oriented concepts such as inheritance, and create Java programs that work  more...

Introduction to C# 2008 Training ...rn all the language features that you must internalize in order to create full-featured Web or Windows applications that make best use of the .NET platform.You will learn about data types, variables, and operators, along with all the important flow control structures. You will work through several examples demonstrating the power of the .NET Framework 3.5, and dig into creating and consuming  more...

MOC 6420 - Fundamentals of Windows Server 2008 Network and Applications Infrastructure ...ts 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 Desktop Support workers moving into server support. The information in this course allows them acquire a fundamental understanding of Windows networks to pursue advanced  more...

How to Dramatically Improve the Quality of Your Shipment ForecastsTechniques to Improve Forecast Inputs ...e of equally considering past, present and future data in order to understand the direction and projected magnitude of customer shipments. 3. Learn what future information goes into a a Market Requirements Definitiona (MRD) document and how it should be created and maintained. 4. Learn how to better use past shipment data to more closely predict future shipments. 5. Learn the  more...

The Most Important Metrics For Measuring Supply Chain Performance ...ivities. Common cycle time metrics include: a Customer Order Promised Cycle Time a Customer Order Actual Cycle Time a Manufacturing Cycle Time a Purchase Order Cycle Time a Fill Ratea the rate or quality of completing a required or set of required activities. Common fill rate metrics include: a Line Count Fill Rate a SKU Fill Rate a Case Fill Rate a  more...

How to Conduct an Effective Monthly Variance Review Meeting ...have a tendency to routinely review, include: + Closed Order Variances + Purchase Price Variances (PPV) + Burden Absorption Variances + Labor Absorption Variances + On-Time Completion Variances + Cycle Time & Throughput Variances + Yield Variances This 1-hour FREE webinar will address how great plant managers prepare for and conduct their variance review meetings and what  more...

Better Methods for Maintaining Accurate Operation Standards ...are the cornerstone of successful capacity planning, work order control, process flow planning and cost accounting. There are few data elements in a manufacturing company's database that require the attention that operation standards require. This LIVE and INTERACTIVE 90-minute workshop will present several ideas for better maintenance of these standards. The instructor will share methods  more...

Should Under-Utilized Capacity Costs Be Included in Work Center Burden Rates The Manufacturing Executive Institute is pleased to bring you this LIVE & FULLY interactive 90-minute "Virtual Classroom" webinar," Should Under-Utilized Capacity Be Included in Work Center Burden Rates?" When your factory is underutilized, your productsa ™ incremental fixed cost is increased. As your factory gets more utilized, the allocated incremental fixed-costs decrease, thus  more...

Supervision in Clinical Traumatology ...pants must complete courses TI-1001 & TI-202 to TI-207 in order to enrol in this course. OBJECTIVES: Supervision in Clinical Traumatology offers a framework for participants to practice and demonstrate proficiency in clinical traumatology skills. The program is offered in a format designed to challenge and help participants grow into competent providers of care for traumatized individuals,  more...

Early Intervention Field Trauma Training First responders (e. g., fire/ rescue, emergency medical services, law enforcement) as well as mental health and health care professionals will benefit from Field Trauma training. This is an entry-level program and no pre-requisites are required to receive the Field Trauma designation other than successful course completion. Participants will learn about on-site responding and learn how to respond  more...

Keeping Work Order and Purchase Order Due Dates Accurate - A Key to Production Planning Success ...oes your company, at this very moment, have past due work orders or purchase orders? Does your company utilize a priority planning system (MRP, KanBan, etc.) to manage the flow of materials through the factory? Does your company have a materials management organization that responds to expedite activity more than to planned activity? This FREE 1-hour webinar will present some new thoughts  more...

New Final HIPAA Amendments New final rules for HIPAA Expand the Scope and Increase Responsibilities ...d when, and what to keep in mind as they move forward, in order to be prepared for compliance with the new regulations. It will provide a comprehensive look at the changes in the law and prepare attendees for the process of incorporating the 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  more...

Risk Assessment - Compliance Using Easy To Fill Out Documentation - Webinar By GlobalCompliancePanel This webinar teaches how to determine and document risk in a process in order to reduce validation time and ensure compliance. Tuesday, February 21, 2012 10: 00 AM PST | 01: 00 PM EST  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...

Audits In The Health Care Industry - Getting Ready for an Outside Audit - Webinar By mentorhealth You need to attend in order to control your own destiny. Get involved up front instead of being a "sitting duck". Tuesday, October 11, 2011 10: 00 AM PDT | 01: 00 PM EDT  more...

Implementing a Quality Systems-Based Approach to GCP Compliance - Webinar By GlobalCompliancePanel Ensuring GCP quality has often been approached from the perspective of reviewing as many documents as possible, looking for errors and following up on corrections or making "notes to file." In order to design, implement, and maintain GCP compliance in an effective manner, a Quality Systems Approach should be adopted.  more...

Risk Assessment - Compliance Using Easy To Fill Out Documentation BY GCP This webinar teaches how to determine and document risk in a process in order to reduce validation time and ensure compliance  more...

Document Retention and Destruction ...ould be kept and when and how they should be destroyed in order to stay in compliance. Effective Human Resource Departments should have a documented Plan to manage employee records safely and effectively. Why should you attend: In order to be in compliance with recordkeeping compliance you should review your policies and practices on record retention and destruction on a regular basis. This  more...

Coaching and Mentoring for High Performance by TrainHR ...e critical skills that every manager should be engaged in order to develop the competence and confidence of employees. Great organizations achieve their full potential because they have exceptional people. But few people are born great. Nor are most people exceptional the day they begin work. They become high performers after they have been trained and given the opportunity and encouragement  more...

Effective Employee Performance Documentation Elements and Techniques by TrainHR Communicate better, improve performance, and defend yourself from legal challenges by producing more effective performance documentation. Employees are more productive when they know what is expected of them. Employee discipline is easier when documents are in order, and high standards are met when directions are clear. Learn simple, stress-free methods for collecting the right information,  more...

Failure Mode Effects Analysis FMEA - The Tool of Choice to Improve Product and Process Reliability and Efficiency While Reducin Failure Mode and Effects Analysis is a tried an proven technique to improve the quality, reliability and safety of products and processes in a proactive manner. It has been used successfully for over 60 years in very type of industry and in all stages of product development, process improvement projects. It helps to increase customer satisfaction, by proactively addressing failures that keep us  more...

Document Retention and Destruction by TrainHR You should attend this webinar to be sure both you and your staff in charge of records understands the responsibility and importance of knowing and following proper procedures. When auditing how information is kept by Human Resource Departments, many questions come up regarding where records are kept, how long they should be kept and when and how they should be destroyed in order to stay in  more...

DHF DMR DHR Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel ...ate Design Control and the Design History File (DHF). In order to sell globally, the EU's CE-marking documentation is a requirement - the Technical FiIe or Design Dossier. Currently they serve different purposes, support different goals, but the TF/ DD is moving in the direction of the DHF. And the DHF is adapting to some of the features of the TF/ B9DD. Being aware of the similarities and  more...

Information Security Risk Analysis Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePane ...alysis 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 process. Areas Covered in the Session: * Learn how to conduct an information security risk analysis suitable to aid in compliance with the HIPAA Security Rule and other information security regulations relevant to health information managers.  more...

Root Cause Analysis - The Heart of a Successful CAPA Program - Webinar By GlobalCompliancePanel ...often improperly dismissed arbitrarily. It is required in order to "close-the-loop" on corrective and/ or preventive actions, and do proper impact analysis / actions. As such RCA is a major element of cGMP compliance, and is also a key source of regulatory problems. How can companies allocate scarce resources to those activities that have the greatest impact to product quality / safety,  more...

Gowning Systems Used in Cleanrooms Controlled Environments - Webinar By GlobalCompliancePanel ... the garments can also vary and needs to be controlled in order 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  more...

Navigating the Regulatory Environment for the Implementation of Alternative Microbiology Technologies - Webinar By GCPanel ...s, it is necessary to work with regulatory authorities in order to effectively introduce a RMM in place of an existing microbiology method. This is especially true if the existing method is incorporated in a previously approved regulatory dossier, such as a New Drug Application (NDA) or Marketing Authorization. There are different perspectives on RMM validation, submission and implementation  more...

Controlled Substances and the Hospital Pharmacy - Webinar By GlobalCompliancePanel ...stances in a hospital setting and many recommendations in order to be in full compliance with the DEA regulations. * Storage and Dispensing: This section covers the storage and dispensing of controlled substances from the pharmacy to the many sections within the hospital including patient wards, emergency rooms and surgical areas. * DEA Recordkeeping Requirements: This section covers  more...

Validating Rapid Microbiological Methods - Webinar By GlobalCompliancePanel ...rview of how to design a meaningful validation program in order to effectively demonstrate that the new RMM is suitable for its intended use and is equivalent to, or better than, the existing method you intend to replace. Topics will include the development of User Requirements Specifications, the validation master plan, IQ, OQ and PQ expectations, and a comprehensive review of how to utilize  more...

Best practices for conducting OOS investigations - Webinar By GlobalCompliancePanel ...o help the attendees clearly understand the steps and the order in which they are to be performed. 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  more...

XML Training ... XSD INDICATORS What are they? Types of Indicators Order indicators Occurrence indicators Group indicators Examples of Indicators 9. EXTENDING XML DOCUMENTS What is it? The element The element Examples 10. BUILDING A XSD FILE A FULL EXAMPLE XML document Building the schema Full schema file Other ways of writing the schema XML Canonical Data Model  more...

Project Management for Clinical Trials - Webinar By GlobalCompliancePanel ...ck availability of study medication and place provisional order so as to prevent this becoming a rate limiting activity. The exact quantities can be refined later. Ensure the qualified person (QP) has been contacted in order to help prevent delays in obtaining the study medication * Prepare a contingency plan for unavailability of comparator drugs in some countries. * Decide on  more...

Controlled Substances and the Pharmacist - Webinar By GlobalCompliancePanel ...filled the prescription. The pharmacy may be inspected in order to determine their handling of controlled substances purchased and dispensed as a prescription. The inspection targets record-keeping requirements, security of all controlled substances, and review of dispensed prescriptions. Class participants will familiarize themselves with federal laws and DEA regulations requirements for  more...

Preparing for GFSI and other Third Party Audits - Webinar By GlobalCompliancePanel ... are requesting pre-assessments to prepare for audits. In order to work cost effectively, allocating resources and dollars to professional help with developing better systems rather than simply reviewing current programs, the supplier will be given the tools necessary to do its own preassessment and gap analysis. Audit results are as much a function of proper preparation as day to day  more...

Internal Audits Maintaining your Quality Systems at the Ready - Webinar By GlobalCompliancePanel ... Untimely repairs affect productivity as well as customer order fulfillment. A systematic approach to maintenance is critical to operations, quality and safety. Areas Covered in the Session: * How to prepare an audit policy and program * A sample checklist for documenting audit results * What to look for * Where to look * Establishing evidence of corrective  more...

New Changes to HIPAA The latest changes in the regulations and what they mean to you - Webinar By GlobalCompliancePanel ...d when, and what to keep in mind as they move forward, in order to be prepared for compliance with the new regulations. The teleconference will provide a comprehensive look at the changes in the law and prepare attendees for the process of incorporating the changes into how they do business in their facilities. Business associates are now directly covered by the HIPAA privacy and security  more...

Preventive and Corrective Maintenance Protect your assets Protect your consumers - Webinar By GlobalCompliancePanel ... Untimely repairs affect productivity as well as customer order fulfillment. A systematic approach to maintenance is critical to operations, quality and safety. Areas Covered in the Session: * Preventive Maintenance * Corrective Maintenance * Post repair sanitation * Equipment catalog * Chemical control * Tools and parts control * GMP for maintenance  more...

Medical Device Tracking Latest FDA Update and Expectations - Webinar By GlobalCompliancePanel ... that manufacturers track certain devices when the agency orders them to do so. Tracking is intended to facilitate notification and recall in the event a device presents a serious risk to health that requires prompt attention. The tracking provisions enacted by SMDA required mandatory tracking even if FDA did not issue an order. Specifically, section 519(e), as added by SMDA, required  more...

FDA 483 Observations in the Laboratory What went wrong How can they be avoided - Webinar By GlobalCompliancePanel ...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. In this webinar we will focus on the laboratory and recent FDA laboratory based operations. We will review observations, identify the real issue  more...

Know Your Customer - The DEA Due Diligence - Webinar By GlobalComplaincePanel This training will cover several recommendations to improve Due Diligence when distributing Schedules II through V controlled substances and regulated chemicals to your customers and what steps can be taken to prevent the illicit use or diversion of any product sold to a customer. As a firm handling these products, you will get a better understanding of what is required from a DEA registered  more...

Navigating Pediatric Trials from recruitment to successful on-time completion - Webinar by GlobalCompliancePanel ...ials come with a high level of complexity and cost. In order for professionals to carry out a successful pediatric drug development plan, they need the right infrastructure and information to avoid obstacles such as slow recruitment, noncompliance and difficulties in developing the right study criteria and protocol. When conducting research on children, drug companies must ensure that  more...

Managing the IDE Investigational Device Exemption Submission for Compliance Success - Webinar by GlobalCompliancePanel ... investigational device to be used in a clinical study in order to collect safety and effectiveness data required to support a Premarket Approval (PMA) application or a Premarket Notification [510(k)] submission to FDA. Clinical studies are most often conducted to support a PMA. Only a small percentage of 510(k)'s require clinical data to support the application. Investigational use also  more...

Failure Modes and Effects Analysis FMEA - An Effective Tool for Medical Device Risk Management - Compliance Webinar by GlobalCom The presentation will discuss the proper use of FMEA in risk management and how to recognize and avoid the traps associated with this tool in order to have a more efficient risk management process.  more...