USP General Chapter 797> describes a number of requirements, including responsibilities of compounding personnel, training, facilities, environmental monitoring, and storage and testing of finished preparations.
Quality solutions at a glance—navigate quickly through USP standards and materials for critical Active Pharmaceutical Ingredients (APIs) and Excipients, all in one Place using our Quality Solution Sheets (QSS). The QSS is a single resource that integrates monographs associated with an API or Excipient with all relevant general chapters, Reference Standards, Pharmaceutical Analytical ...
JD Supra: Status of USP Chapter 800 Becomes More (and Less) Clear Following USP Appeals Panel Decision
On , an Appeals Panel of the United States Pharmacopeial Convention (“USP”) granted appeals to revisions of two compounding standards—General Chapter <795> Pharmaceutical Compounding – ...
Status of USP Chapter 800 Becomes More (and Less) Clear Following USP Appeals Panel Decision
The U.S. Pharmacopeia Appeals Panel sent two revised compounding chapters back to an expert committee for review March 12. The two revised chapters are USP chapter 795, which regulates nonsterile ...
Becker's Hospital Review: USP Chapters (797) and (800): Updates and Compliance Tips for Hospitals
PharmTech: USP Announces Monograph Revisions List and Postponed Publication of General Chapter <1226>
USP Announces Monograph Revisions List and Postponed Publication of General Chapter <1226>
The United States Pharmacopoeia (USP) has released a new draft chapter proposing a set of analytical procedures and best practices to accelerate product development and support quality assessments for ...
A revised version of the USP chapter on Total Organic Carbon (TOC) USP<643> was published recently and will become official on 1 st May 2021. This paper gives an overview of this new USP chapter and ...