We will selectively include calls for public consultation from multilateral agencies, governments, INGOs and other sources where there is a clear intersection with consent/assent. This might be obvious from the title of the draft guidance, regulations, etc., but more often, it will be a thematic area or topic – if properly addressed at all. If you would like to explore participation with our working group developing submissions for these calls, please contact us [david.r.curry@ge2p2global.org].
Public Consultation: ICH E6(R3) [GCP] Principles, Annex 1 and Annex 2
ICH – The E6(R3) EWG is working on the revision of the E6(R2) Guideline “Good Clinical Practice” (GCP) with a view to addressing the application of GCP principles to the increasingly diverse trial types and data sources being employed to support regulatory and healthcare related decision-making on drugs, and provide flexibility whenever appropriate to facilitate the use of technological innovations in clinical trials.
Public consultation dates:
ANVISA, Brazil – Deadline for comments by 31 August 2023
EC, Europe – Deadline for comments by 26 September 2023
FDA, United States – Deadline for comments by 5 September 2023
HSA, Singapore – Deadline for comments by 30 September 2023
Health Canada, Canada – Deadline for comments by 20 October 2023
MHLW/PMDA, Japan – Deadline for comments by 9 September 2023
MHRA, UK – Deadline for comments by 31 August 2023
NMPA, China – Deadline for comments by 31 August 2023
Swissmedic, Switzerland – Deadline for comments by 26 September 2023
TFDA, Chinese Taipei – Deadline for comments by 31 August 2023
Public consultation on WHO guidance for best practices for clinical trials
WHO -19 July 2023
Call for consultation: Deadline 15 Sep 2023
WHO launches a global stakeholder survey on solutions for strengthening clinical trial infrastructure and capacity
This global stakeholder survey will be open until 10th September 2023.
The outcomes of the public consultation and the global survey will guide the WHO in a series of upcoming regional and global consultations with Member States and non-State-actors towards the implementation of the WHA resolution 75.8 on clinical trials.