Clinical Laboratory Incident Management Plan - GLP and FDA Compliance 2013

  • 26 Feb 2013
  • Webinar

Description

GLP and Compliance for a Clinical Laboratory’s Incident Management Plan is a webinar that covers topics such as:

  • The Three Phases of Testing
  • Quality Assurance vs. Quality Assessment: Why the Change?
  • Quality Control: Principles and Practice
  • Quality Assessment Systems That Work
  • QC Formulas and Their Use
  • QC for Waived Testing: Is Minimum Enough?
  • Measurement indicators for QA
  • Why QC and QA are linked processes

GLP and Compliance for a Clinical Laboratory’s Incident Management Plan brings together:

  • Compliance Officers
  • Administrators of Clinical Laboratories
  • Administrative Laboratory Director and Managers
  • Quality Assurance Personnel
  • Risk Management Personnel
  • Medical Directors and Pathologists

Past Events

Important

Please, check "Clinical Laboratory Incident Management Plan - GLP and FDA Compliance" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical laboratories
Science: Laboratories

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