• 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


To Order:

Simply Call: 07955 680944 & quote E6 (R2)


Fill out a formscan it to office@icr-global.org or send it to The Institute of clinical research,White Waltham, Maidenhead SL6 3LW

Technical Detail


86 pages