Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018

Date : 8th January 2018 to 9th January 2018

Place : Switzerland, zurich, switzerland

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901444SEMINAR?allconferencealerts-January-2018-SEO

Contact Person:Event Manager

Description:

Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and / or international regulations or business continuity requirements. In addition, the FDA has stepped up 21 CFR 11 inspections that include CSV. This course will build on the Validation and 21 CFR 11 Compliance

Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018 will be held in zurich, switzerland,Switzerland on date 2018-01-09

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Deadline for abstracts/proposals : 7th January 2018

Keynote Speakers : Angela Bazigos is the CEO of Touchstone Technologies Inc. She has 40 years of experience in the Life Sciences & Healthcare Industries. Experience combines Quality Assurance, Regulatory Compliance, Information Technology, Project Management, Clinical Lab Science, Microbiology, Food Safety and Turnarounds. Past employers / clients include Roche, Novartis, Genentech & PriceWaterhouseCoopers, Public Health Service. Positions include Chief Compliance Officer, http://morflearning.com/angelabaz

Conference Highlights :Pharmaceuticals Biotech Medical Device Radiological Health Blood Products Companion Animals Food Cosmetics Tobacco Academia

Venue :Zürich, Switzerland

Check the event website for more details.