BEGIN:VCALENDAR X-WR-TIMEZONE:US/Eastern DTSTART:20200211T130000 DTEND:20200211T143000 VERSION:2.0 LOCATION:OnlinePRODID:-//Training Doyens //EN METHOD:REQUEST BEGIN:VEVENT DTSTAMP:20200211T000000 DTSTART;TZID="US/Eastern":20200211T130000 DTEND;TZID="US/Eastern":20200211T143000 SUMMARY:Good Documentation Practices to Support FDA Computer System Validation DESCRIPTION: FDA requires that all documentation related to GxP products (GMP, GLC, GCP) be created and maintained in accordance with specific rules. From the color of the ink used to the retention requirements, you’ll learn all about how to create and maintain good FDA-compliant documentation. The webinar will leave you with the information needed to create and maintain good documentation that meets FDA compliance standards. You will learn about what must be done and what must not be done. In addition, you’ll learn about the various computer system validation guidelines, deliverables and how to document them. PRIORITY:3END:VEVENT END:VCALENDAR