BEGIN:VCALENDAR X-WR-TIMEZONE:US/Eastern DTSTART:20190206T130000 DTEND:20190206T143000 VERSION:2.0 LOCATION:OnlinePRODID:-//Training Doyens //EN METHOD:REQUEST BEGIN:VEVENT UID:20190206T000000-1206134444-example.com DTSTAMP:20190206T000000 DTSTART;TZID="US/Eastern":20190206T130000 DTEND;TZID="US/Eastern":20190206T143000 SUMMARY:In-Depth Testing of Computer Systems Regulated by FDA DESCRIPTION: FDA requires that all documentation related to GxP (GMP, GLC, GCP) products be created and maintained in accordance with specific rules. From the color of the ink used to the FDA labeling 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 validation deliverables for computer systems regulated by FDA and how to document them through the entire process. PRIORITY:3END:VEVENT END:VCALENDAR