ROCKVILLE, Md., June 3, 2019 /PRNewswire/ -- USP released new and revised standards to help ensure the quality of compounded medicines. The updates pertain to the USP General Chapters on compounding ...

The organization’s goal in this area is to provide suitable methods and reference standards that can help the industry and regulators ensure cannabis quality The U.S. Pharmacopeia (USP) has decided to ...

Ganeden Biotech is pleased to announce that GanedenBC 30 (Bacillus coagulans GBI-30, 6086) is the first probiotic to have a monograph published in the Food Chemical Codex (FCC) from the U.S.

This report provides plans for the USP Council's work in the 2010-2015. This articles contains online bonus material. USP s compendia and reference materials are made available through decisions of ...

While many health systems have taken steps to address these new standards, developing a proactive strategy can be challenging. Leveraging IV compounding automation to streamline cleanroom processes ...

The U.S. Pharmacopeia (USP), the world's only nongovernmental pharmacopeia, establishes state-of-the-art standards to ensure the quality of medicines, dietary supplements, and other healthcare ...

This will allow quality specialists to integrate standards into digital workflows with greater efficiency, consistency, and reduced risk.

On Nov. 1, the new U.S. Pharmacopoeia standards on sterile and nonsterile compounding will be implemented. Here’s what leaders need to know about USP 795 and USP 797: a. Nonpreserved aqueous dosage ...

USP is developing and revising distribution standards in response to changes in the global supply chain. Today, it is common for pharmaceutical products to be sourced in a complex maze of processing ...

The United States Pharmacopeia (USP) Convention’s Chapter 800, “Hazardous Drugs — Handling in Healthcare Settings,” goes into effect Dec. 1. The new standards provide detailed specifications for the ...

The USP 800 requires ASCs and other healthcare organizations to be compliant with a number of medication handling standards regarding receiving, transporting, storing, dispensing and disposing of them ...

The U.S. Food and Drug Administration today alerted health care professionals to a change in heparin manufacturing that is expected to decrease the potency of the common anti-clotting drug. To ensure ...