Definitions Web-based Seminars

Top Tips For Managers to Prevent Harassment in your Workplace ...earning Objectives This presentation will cover: a Definitions of Quid Pro Quo and Hostile Work Environment Harassment a Mistakes Managers Make that can Create a Hostile Work Environment in your Workplace a Tips For Avoiding a Hostile Work Environment a It's Not Just About Sex Anymore-Hostile Work Environments Based on Protected Classes Other than Sex a Tips to Avoid  more...

SharePoint 2007 Development Training This advanced SharePoint training class focuses on the SharePoint Developer and targets developers who need to customize SharePoint at a core level. The course focuses on Windows SharePoint Services 3.0 (WSS) fundamental building blocks such as features, application pages, site pages, Web Parts, custom list types, site columns, content types, custom workflows and site definitions. You will also  more...

Understanding Improving Yields Scrap Rework ...result. This FREE 1-hour webinar presents the CORRECT definitions of yield, scrap 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?  more...

Verification vs Validation in Regulated Industries - webinars by gcp Attend this webinar to understand the differences and benefits of verification and validation. Learn about the risks and complications involved with the application of sound verification and validation principles.  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 ...reas 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 Will Benefit: RA Directors, Managers and Staff QA Directors,  more...

Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine This webinar will provide valuable assistance to all device manufacturers, those who market solely within the US, or those who wish to market in the EU as well  more...

Recalls Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel ...tors. 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 - Canada & Europe Who Will Benefit: *  more...

Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ...on: * 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 (DMR) o Definition o Typical contents o DMR and  more...

A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - W ...uality Systems Approach * Module 6 - A Comparison of Definitions and Terms * Module 7 - Comparison of Personnel and Management Expectations * Module 8 - Comparing Design Requirements * Module 9 - Comparing Master Records * Module 10 - Comparing Equipment Controls * Module 11 - Comparing Material and Incoming Controls * Module 12 - Comparing the Control of  more...

HIPAA Business Associates How the regulations have changed and what you need to do for compliance now - Webinar By GCPanel ...s of Changes to Business Associate Rules o New Definitions of Business Associates o Contractors of Business Associates * New Requirements and Changed Requirements for HIPAA Business Associates o HITECH Act Required Capabilities o Required Amendments to BAAs o BAA Provisions to Consider o Transitioning to the New Rules *  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...

Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel ... o General requirements for records o Definitions from Part 11 + Electronic records + Closed systems + Open systems o Summary of requirements + Validation + System access + Audit trail + Other requirements o The guidance document  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 ... assign a CAPA to an individual o Examples and definitions of teams and team members roles and responsibilities o It can be used and applied in other areas inside and/ or outside the organization when and where team work is required and expected o This section by itself can be taken out and applied to other processes and practices within or outside of the  more...

Food Safety Management Systems - ISO 220002005 - Webinar By GlobalCompliancePanel ...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 Assessment - Control Measures * Design and Redesign of HACCP Plan a Critical control points  more...

Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ...on: * 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 (DMR) o Definition o Typical contents o DMR and  more...

New Changes to HIPAA The latest changes in the regulations and what they mean to you - Webinar By GlobalCompliancePanel ...m of $10, 000 and can go up to $1. 5 million or more. The definitions of the penalty levels include new definitions for reasonable cause and reasonable diligence, as well as willful neglect, which have a direct impact on the amount of penalty a violation may be subject to. Electronic records have new demands placed on them, in both providing access and in accounting for all disclosures of  more...

Recalls Removals and Market Corrections in Compliance with FDA and ISO Requirements - Webinar By GlobalCompliancePanel ...uct. 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 13485-specific requirements * CMD-specific  more...

Revamping the 510k Clearance Process-Understanding FDAs Proposals - Webinar by GlobalCompliancePanel ...could streamline the clearance process. There will be new definitions of "Substantial Equivalence" and "intended Use" will be redefined and "Indications for Use" eliminated The FDA will likely increase the requirements for the Summary of Safety and Effectiveness and require a summary of all scientific information known or that should be reasonably known to the submitter regarding the safety  more...

Complete Java Training ...nd Stylesheets o Tiles Attributes o Tiles Context o Definitions o Inheritance of Tiles Defination o Custom Definitions J2EE Application Deployment * Development and Administration o Development Process o Assembling WARs o Administrative Tools o Administrative Tasks * Apache Tomcat web server training * Application development and deployment in Apache Tomcat  more...