- By ICR Secretariat
- Posted Thursday, June 22, 2017
Guideline For Good Clinical Practice E6(R2)
A handy pocket/handbag sized guide to E6(R2).
The objective of this ICH GCP Guideline is to provide a unified standard for the European Union (EU), Japan and the United States to facilitate the mutual acceptance of clinical data by the regulatory authorities in these jurisdictions.
The guideline was developed with consideration of the current good clinical practices of the European Union, Japan, and the United States, as well as those of Australia, Canada, the Nordic countries and the World Health Organisation (WHO).
Investigators and Sponsors
Clinical Trial Protocols and Protocol Amendments
Investigators Brochure (IB)
Essential Documents for the conduct of a clinical trial
1 - 5 Copies = £3.00 per copy
11 - 15 copies = £2.80 per copy
16 - 20 copies = £2.75 per copy
21 - 50 copies = £2.60 per copy
51 - 100 Copies = £2.50 per copy
Simply Call: 01628 501700 & quote E6 (R2)
Fill out a form; scan it to firstname.lastname@example.org or send it to The Institute of clinical research,White Waltham, Maidenhead SL6 3JF