Information SystemsSession Type: Recorded Webinars
The increased use of information technology and computer systems in all aspects of business is leading to the automation of more and more processes. Key decisions and actions are routinely being taken using Information Systems (IS), with regulated records being generated and maintained electronically throughout the product life-cycle. This Webinar aims to give the participant practical knowledge of the following:
System types covered include Enterprise Resource Planning (ERP), Manufacturing Execution Systems (MES), Laboratory Information Management Systems (LIMS), and Electronic Document Management Systems (EDMS). The approach is based on guidance published by GAMP – an ISPE Community of Practice. Relevant GAMP Guidance includes the GAMP Guide to Validation of Automated Systems, and the GAMP Good Practice Guide: A Risk Based Approach to Compliant Electronic Records and Signatures. Learning Objectives:
Who should attend:
Speaker Biography Sion Wyn, Director, Conformity Ltd., is an acknowledged expert in computer system validation and compliance and international regulations. He has extensive experience in all aspects of computer systems validation and compliance, including managing validation projects, validation planning, specification and testing of systems, performing site and system compliance audits, writing SOPs, performing 21 CFR Part 11 assessments, and supplier audits. Wyn’s expertise as a specialized computer validation consultant covers all stages of the lifecycle approach to validation of computerized systems and most system types including MRPII, manufacturing execution, electronic document management, EBRS, process control and monitoring, environmental monitoring, manufacturing equipment, and laboratory systems. At Conformity Ltd., Wyn provides computer validation and compliance consultancy to the pharmaceutical and other regulated healthcare industries. What is a Recorded Webinar?Previously held webinars are available as recorded sessions, which you can view at your convenience. Registration orders are processed within two business days, after which participants will receive an email confirmation with a link to the Recorded Webinar. After receiving the link to the Recorded Webinar, you have 15 days to view it. What are CPIPSM Recorded Webinars?CPIPSM Recorded Webinars are a group of Recorded Webinarswas developed to help individuals in preparation for the Certified Pharmaceutical Industry ProfessionalSM (CPIPSM) examination. The Certified Pharmaceutical Industry ProfessionalSM (CPIPSM) credential recognizes “change agents” as the necessary ingredient to foster industry innovation and enhance drug product quality. The credential establishes a global competency standard for industry professionals, and candidates are assessed through demonstrated education, experience, and a rigorous examination. Completion of any of these seminars does not guarantee successful completion of the CPIP certification exam, and these seminars do not include every subject to the depth of what will be covered on the CPIP exam. Page last updated: 11 December 2008 |
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