All regulations
Nonrulemaking
FDA
Open for Comments
FDA-2025-D-2275
M4Q(R2) The Common Technical Document for the Registration of Pharmaceuticals for Human Use: Quality; International Council for Harmonisation; Draft Guidance for Industry; Availability
Documents
2
Comments
18
Key Dates
Comment Period OpensJan 21, 2026
Comment Period ClosesMar 24, 2026
Documents
Comment Statistics
Total Comments
18
Keywords
2022-202
CDER
M4Q R2 The Common
Technical Document for the Registration
Pharmaceuticals for Human Use Quality
International Council for Harmonisation
Draft Guidance for Industry
Availability
Data from Regulations.gov