Note for guidance on good clinical practice.
Material type: TextSeries: ICH Topic ; E6 | Guideline for good clinical practice ; Step 5, Consolidated GuidelinePublication details: London : ICH, 1997. Description: 115 pSubject(s): Clinical trials -- standards | Drug evaluation | Human experimentation | Informed consent | Guidelines | Ethics, Medical | Legislation, Medical | European Union | Japan | United StatesNLM classification: W 20.5 97EUItem type | Current library | Call number | Copy number | Status | Date due | Barcode |
---|---|---|---|---|---|---|
Books | WHO HQ BORROWABLE-COLL-STACKS | W 20.5 97EU (Browse shelf(Opens below)) | 1 | Available | 00065379 |
Browsing WHO HQ shelves, Shelving location: BORROWABLE-COLL-STACKS Close shelf browser (Hides shelf browser)
No cover image available | No cover image available | |||||||
W 20.5 96FR Fundamentals of clinical trials / | W 20.5 96RE Report of the Review of the Role and Functioning of Institutional Ethics Committees : | W 20.5 97CO Les Comités de la recherche biomédicale : | W 20.5 97EU Note for guidance on good clinical practice. | W 20.5 97EU V1 Health research with developing countries : | W 20.5 97EU V1 Health research with developing countries : | W 20.5 97EU V2 Health research with developing countries : |
The Belmont report: ethical principles and guidelines for the protection of human subjects of research.
CPMP/ICH/135/95
4
There are no comments on this title.