Published: Tuesday, April 30, 2019
Event date: 5/28/2019 11:00 AM - 12:30 PM Export event
Good Documentation Practices (GDP) are essential elements in regulated manufacturing and laboratory environments. Personnel in these fields need to closely adhere to GDP to ensure an auditable account of work performed. GDP is required for all documentation included in a fully developed quality system. This live webinar will cover USP–NF General Chapter <1029> and all aspects of GDP, including practices for writing and correcting documentation as well as the various documentation required by U.S. FDA 21 CFR section 11 (electronic records and electronic signatures) as applicable to all stages of product development.
Number of Seats:
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