Auditing Analytical Laboratories for FDA Compliance 2012

  • 28 Nov 2012
  • Webinar

Description

Auditing Analytical Laboratories for FDA Compliance 2012 is a webinar that covers topics such as:

  • Reviewing documentation
  • GMP regulations that apply to analytical laboratories
  • Auditing styles and structures
  • Advance preparation for the audit
  • What to look for while doing a walk-through
  • Equipment and laboratory instrument qualification
  • Following through on the audit
  • Other regulations and standards, including ISO 17025

Auditing Analytical Laboratories for FDA Compliance 2012 brings together Supervisors and Analysts in Quality Control Laboratories and Quality Assurance groups, External and Internal Auditors, Personnel Responsible for Selecting Contract Testing Laboratories, Supervisors and Analysts in Contract Testing Laboratories and Consultants.

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Important

Please, check "Auditing Analytical Laboratories for FDA Compliance" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical laboratories
Science: Laboratories

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