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Printable Handouts
Navigable Slide Index
- Introduction
- OECD council decision - C(89)87(Final)
- GLP compliance monitoring definition
- Annex II to OECD recommendation C(89)87(Final)
- The number of test facilities globally
- Types of research under GLP
- The inspector
- The inspector: revised guidance no. 3
- GLP inspections - frequency
- Implementation inspection
- Compliance monitoring inspection
- For cause inspections
- GLP inspections - announcement
- GLP inspections - number of inspectors
- Pre-inspection
- Regular GLP inspection
- Introductory meeting - who should attend
- Introductory meeting (1)
- Introductory meeting (2)
- Short tour (optional)
- Organisation and personnel
- Quality assurance
- Inspection tour
- Facilities
- Biological test systems (1)
- Biological test systems (2)
- Test systems
- Test and reference items
- Apparatus, materials, reagents, specimens
- Computerised systems (1)
- Computerised systems (2)
- SOPs
- Archiving
- Study audits: study plan vs. performance
- Study audits: final report
- Closing conference
- Definition of deficiencies
- Follow-up to inspections and study audits
- GLP status
- Certificates
- Where serious deviations are found
- Confidentiality
- Appeals procedures
Topics Covered
- Inspection procedures
- The organization of official authorities
- The performance of official authorities
- How to assess compliance with the OECD principles of Good Laboratory Practice
Talk Citation
Helder, T. (2012, March 1). Inspection procedures [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 3, 2024, from https://doi.org/10.69645/PRVF5538.Export Citation (RIS)
Publication History
Financial Disclosures
- Mr. Theo Helder has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.