Products like I-Flow's ON-Q PainBuster postoperative pain relief system are subject to USP <797>. On January 1, 2004, United States Pharmacopeia (USP) Chapter <797> “Pharmaceutical Compounding—Sterile ...

USP 797 went through its final revision approval in December. The new standard becomes official June 1. What is it, who will it affect, and where will it be implemented? The United States Pharmacopeia ...

The author provides a history of the information chapter USP ‹1211› "Sterilization and Sterility Assurance of Compendial Articles," from the early 1900s to the current version. In 1900, the eighth ...

The introduction of the United States Pharmacopeia Chapter <797> regulation in 2008 sent and continues to send shock waves through hospital pharmacy departments and other sterile drug preparation ...

On June 1, 2019, the United States Pharmacopeia (“USP”) published the final revisions to its pharmaceutical sterile compounding standards (“chapter <797>”). Chapter <797> sets forth standards for the ...

Dublin, April 20, 2023 (GLOBE NEWSWIRE) -- The "Microbiological Rapid Method Sterility Testing (RMT) of Short Dated and Other Products" webinar has been added to ResearchAndMarkets.com's offering. USP ...

Sterile compounding practices are increasingly under scrutiny. State pharmacy boards, in tandem with national efforts by accreditation organizations, are raising the stakes on this critical component ...

Increasing competition and decreasing reimbursement for services provided are driving healthcare organizations to seek innovative value-based, patient-safety focused solutions. Hospitals and ...

SALT LAKE CITY, March 04, 2025 (GLOBE NEWSWIRE) -- Nelson Labs, a Sotera Health company and a global leader in microbiological and analytical chemistry testing and advisory services for the medical ...

Closed and disposable sterility testing devices reduce the risk of false positive results during sterility testing. To further prevent such results, some pharmaceutical manufacturers use the device ...