Auditing Analytical Laboratories for FDA Compliance 2018

  • 03 May 2018
  • Webinar

Description

Auditing Analytical Laboratories for FDA Compliance 2018 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 2018 is intended for:

  • 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
  • Consultants

Past Events

Important

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

Event Categories

Business: Internal Audit & Compliance
Government & Global Issues: Law & Regulations
Health & Medicine: Medical laboratories
Science: Laboratories

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