Infos
- 14/02/2011 - FDA: ICH Q8(R2), Q9 et Q10
- 14/02/2011 - EMA: Quality Risk Management ICH q9 et q10
- 14/02/2011 - annex7 r2
- 14/02/2011 - EMA certificates of medicinal products Intructions on how to fill the application form
- 14/02/2011 - Processing/Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling
- 14/02/2011 - Commission Guidelines on Good Distribution Practice of Medicinal Products for Human Use
- 14/02/2011 - ICH-Endorsed Guide for ICH Q8/Q9/Q10 Implementation
- 02/02/2011 - PIC's: Site Master File
- 02/02/2011 - GMP: Chapter 4
- 26/01/2011 - FDA: Guidance for Industry- Process Validation: General Principles and Practices
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