BEGIN:VCALENDAR X-WR-TIMEZONE:US/Eastern DTSTART:20200115T130000 DTEND:20200115T143000 VERSION:2.0 LOCATION:OnlinePRODID:-//Training Doyens //EN METHOD:REQUEST BEGIN:VEVENT DTSTAMP:20200115T000000 DTSTART;TZID="US/Eastern":20200115T130000 DTEND;TZID="US/Eastern":20200115T143000 SUMMARY:Developing a Strategic Approach to FDA Compliance for Computer Systems DESCRIPTION: FDA requires that all computer systems used to produce, manage and report on GxP (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. You’ll learn all about how to create and maintain good FDA-compliant documentation using a strategic approach based on System Development Life Cycle (SDLC) Methodologies.The webinar will leave you with the information needed to plan, execute and document a computer system validation effort that meets FDA compliance standards.  You will learn about what must be done to ensure the system remains in a validated state.  In addition, you’ll learn about the various computer system validation deliverables and how to document them through the entire process. PRIORITY:3END:VEVENT END:VCALENDAR