Good Laboratory Practices - Introduction, Requirements and Tools for Implementation 2010

  • 30 Nov - 01 Dec, 2010
  • Hilton Garden Inn Montreal Airport, Canada

Description

Program Outline

  • Various GLP s: An Overview &Genesis
  • Global Harmonization Initiatives: An Overview of the ICH Process            
  • Good Laboratory Practices Definition and Objectives                                                                                                               
  • Study Director, PI, QAU, Management, Archivist, Sponsor: Roles and Responsibilities in the GLP s (FDA/OECD)
  • Data Management in a Regulated Environment- Chromatographic Data Systems
  • Testing and Report Control
  • Hands on Half Day Interactive Workshop: Development of a GLP Study Protocol
  • Validation of Analytical Software in a Regulated Environment
  • Best Practices for Equipment and Method Verification/Validation
  • Developing Validation Policies and Procedures Suitable for GLP Work

Past Events

Important

Please, check "Good Laboratory Practices - Introduction, Requirements and Tools for Implementation" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical laboratories, Pharma
Science: Life Sciences & Biology

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