Release of Draft (Step 2) International Council for Harmonisation of Technical Requirements for the Registration of Pharmaceuticals for Human Use Guidance: E17: Principles on planning/designing Multi-Regional Clinical Trials
July 29, 2016
Our file number: 16-108210-816
The above referenced draft guidance was released by the ICH Steering Committee for consultation and is being posted on the ICH website for information and comment in accordance with Step 2 of the ICH process.
Please note that draft guidance documents are only made available in English until finalised by the ICH. It is also important to note that amendments to draft documents may occur as a result of regulatory consultations and subsequent deliberations within the ICH.
All comments forwarded to Health Canada will be transmitted to the ICH as is, with the disclaimer that they are provided for information and do not necessarily represent the views of Health Canada, except as specifically indicated in separate comments.
As appropriate, your organization may alternatively wish to provide comments to your affiliate association in the United States, Europe or Japan for their input directly to ICH.
Comments provided to Health Canada should be submitted by October 27, 2016 in order to allow sufficient time for their assessment and subsequent transmission to the ICH.
Comments should be directed to:
Health Canada ICH Secretariat
Bureau of Policy, Science and International Programs
Therapeutic Products Directorate
Health Products and Food Branch
1600 Scott Street, Tunney's Pasture
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