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Wednesday, January 19, 2022
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Verification and Validation - Product, Equipment/Process, Software and QMS
January 18, 2022 at 9am to January 19, 2022 at 4pm – online Develop / review a company's Master Validation Plan for major cGMP deficiencies. Address the U.S. FDA's newer and tougher regulatory stance. One major failing is lack of sufficient or targeted risk-b… Organized by Complianceonline | Type: seminae
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Statistical Elements of Implementing ICH Guidelines
January 19, 2022 at 10am to January 20, 2022 at 4pm – online Why Should You Attend: Most organizations have programs and procedures but they contain holes or fall short in the implementation of the tools and techniques used to apply proper statistical reasonin… Organized by Complianceonline | Type: seminae
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