New Details on the Revision of USP Chapter 1
![Granulation & Tableting - Live Online Training](files/eca/userImages/training.img/Z-ECA-Granulation-Tableting-2024-Live-Online.jpg)
Recommendation
17-19 September 2024
GMP Compliance and Technology for the Manufacture of Oral Solid Dosage Forms
As already reported in the news "Second Revision of USP Chapter <1> Injections and Implanted Drug Products (Parenterals)-Product Quality Tests", USP's Chapter <1> "Injections and Implanted Drug Products (Parenterals)-Product Quality Tests' has been revised again. New information is now available.
The USP published these details on 25 March. The revised version now contains a table of contents for a better overview whereas the Product Performance Test at the end of the Chapter has been deleted. All details about the new version of USP's Chapter <1> can be found on the USP website.
The revised Chapter will become effective on May 1st, 2016.
Related GMP News
24.07.2024EDQM publishes updated Ph.Eur. Water Monographs for comment
10.07.2024The EU GMP Annex 1 (2022) and the 5 µm Particles in Grade A & B
03.07.2024FDA publishes Final Rule on Medical Gases
26.06.2024Testing of Medicinal Products is no Evidence against Cross-Contamination
19.06.2024Warning Letter to Indian Sterile Manufacturer due to egregious GMP Deficiencies
12.06.2024Requalification of an Automatic Inspection System (AVI)