Seminar - Online
This webinar will provide valuable guidance to medical device manufacturers on how to establish and justify limit values for cleanliness.
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Science Researcher Update: Spotlight on Meetings, Conferences, and Events
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Tags: Medical Device Technology, Medicine, Webinar, May, 2015, Seminar, Life Sciences
Seminar - Online
Risk Elimination. Risk Management. Risk Mitigation. This is the language of upper management, that we as auditors from any industry must learn, if we truly want to effect positive change throughout our environment.
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Tags: Webinar, May, Quality Control, 2015, Seminar, Biologics
Seminar - Online
This webinar presents important facts to simplify the planning and execution phase in your journey towards becoming a combination device manufacturer by incorporating the essential quality system requirements in your company.
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Tags: Medical Device Technology, Canada, Webinar, May, Quality Control, 2015, Seminar
Seminar - Online
This webinar provides some practical and useful answers to this question.
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Tags: Webinar, May, pharmaceutical, 2015, Seminar, biotech industry, Biologics
Seminar - Online
This webinar will focus on the difference between Verification vs Validation and how can we use them to improve the bottom line.
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Seminar - Online
In Dec. 2010, the FDA has stepped up enforcement for 21 CFR 11 compliance with spreadsheets being considered as low hanging fruit for FDA inspectional findings.
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Spotlight on Science Meetings, Conferences and Events brings you information on the following event: Webinar on Laboratory Accreditation: Getting there is Just the Beginning
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Tags: June, Webinar, 2015, Biologics, June 2015, Quality Management System
Seminar - Online
The regulatory background for the Pharmaceutical industry as a whole now requires a ‘risk based approach’ to all activities and that will of course include Outsourcing.
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Tags: Canada, Webinar, May, pharmaceutical, 2015, Seminar, Biologics
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