recherche clinique

Bonnes pratiques cliniques

Bonnes pratiques cliniques

La description: 
The tripartite harmonised ICH Guideline was finalised under Étape 4 in May 1996. This Good Clinical Practices document describes the responsibilities and expectations of all participants in the conduct of clinical trials, including investigators, monitors, sponsors and IRBs. GCPs cover aspects of monitoring, reporting and archiving of clinical trials and incorporating addenda on the Essential Documents and on the Investigator's Brochure which had been agreed earlier through the ICH process.
Implementation
Étape 5
États-Unis:
Adopted by CPMP, juillet 1996, issued as CPMP/ICH/135/95/Step5, Explanatory Note and Comments to the above, issued as CPMP/768/97
MHLW:
Adopted March 1997, PAB Notification No. 430, MHLW Ordinance No. 28
FDA:
Published in the Federal Register, 9 Peut 1997, Vol. 62, Non. 90, p. 25691-25709
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certificat GCP

Norme GCP

Norme GCP («Bonnes pratiques cliniques», Bonnes pratiques cliniques , GOST R 52379-2005) - norme internationale de normes éthiques et qualité de la recherche scientifique, décrivant les règles de développement, effectuer, documentation et rapports de recherche, qui impliquent la participation humaine Lire la suite…

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thérapie de cellules souches