Draft ich guideline e6 on good clinical practice ( pdf/ ich gcp e6 pdf 359. e6 good clinical practice: consolidated guidance introduction good clinical practice ( gcp) is an international ethical and scienti■c quality standard for designing, conducting, recording, and reporting trials that involve the participation of human subjects. ich harmonised guideline good clinical practice ( gcp) e6( r3) international council for harmonisation of technical requirements for pharmaceuticals for human use ich harmonised guideline good clinical practice ( gcp) e6( r3) draft version endorsed on currently under public consultation. guideline for good clinical practice e6( r2) current step 4 version dated 9 november e6( r1) document history first codification history date new codification november e6 approval by the steering committee under step 2 and release for public consultation. 27 april 1995 e6 e6 approval by the steering committee under step 4. additionally, the general ich process will be presented with a focus on the ich e6( r3) development process. department of health and human services. 02 kb) draft first published: ema/ chmp/ ich/ 337843/ revision 1 ich guideline for good clinical practice e6 ( r2) 4 - step 2b ( pdf/ 681. ich e6 principles ( draft version: march ). 68 kb) draft: consultation closed. the ich e6( r3) ewg is organizing a web conference to present the current draft of the gcp principles as a work in progress. e6( r2) good clinical practice: integrated addendum to ich e6( r1) guidance for industry.