Guideline on the regulation of medicinal cannabis in New Zealand: Part 3 (Section 3.2.2) Guideline on the Regulation of Therapeutic Products in New Zealand: Labelling of Medicines and Related Products (Section 2.2 and Figure A).; (33 page(s), in English), (19 page(s), in English)

Certain Existing Chemicals; Request To Submit Unpublished Health and Safety Data Under the Toxic Substances Control Act (TSCA); (7 page(s), in English)

Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006 (COM(2023)193 final); (182 page(s), in English), (37 page(s)