Printable Handouts

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Navigable Slide Index

1. Introduction
2. Talk outline
3. Definition of GLP
4. Objectives of GLP
5. GLP vs. ISO 17025 (1)
6. GLP vs. ISO 17025 (2)
7. History of GLP (1)
8. History of GLP (2)
9. Legal framework of GLP in the EU (1)
10. Legal framework of GLP in the EU (2)
11. Legal framework of GLP in the EU (3)
12. Legal framework of GLP in the EU (4)
13. The role of the member states (1)
14. The role of the member states (2)
15. The role of the member states (3)
16. GLP labs in the EU (2009)
17. GLP in the EU-practicalities
18. Role of the GLP commission inside the EU
19. The GLP web site
20. Foreign relations (1)
21. Foreign relations (2)
22. OECD (1)
23. OECD (2)
24. Relevant agencies
25. EMA GLP inspections
26. Cooperation with receiving authorities
27. Costs and benefits of GLP
28. Conclusions
29. Thank you

Topics Covered

• Good Laboratory Practice
• Definition and development
• Differences and similarities to laboratory accreditation
• The role of the EU Member States, the European Commission and the OECD
• Cooperation with European agencies and regulatory authorities

Links

Series:

• Good Laboratory Practice

Categories:

• Methods
• Pharmaceutical Sciences

Talk Citation

Publication History

• Published on March 1, 2012

Financial Disclosures

• Mr. Maik Schmahl has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.