Good Documentation Practices for Laboratory Operations - Webinar By GlobalCompliancePanel 2011

  • 01 Jun 2011
  • Webinar

Description

The webinar brings together Metrology personnel, QA Auditors of Laboratory Documents, Laboratory Managers, Laboratory Supervisors, Laboratory Technicians, Chemists and Analysts and covers areas such as FDA Investigator strategies, OOS Documentation Expectations, Entering numerical data, Blanks, Handling raw data (charts, strips, printouts), Comments and explanations, Use of "NA", Meanings of initials and signatures, Dates and formats, Correcting errors and omissions, 21CFR and Eudralex references to documentation.

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Event Categories

Health & Medicine: Medical laboratories, Pharma
Industry: Chemical
Science: Laboratories

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