Gene therapy represents one of the fastest growing biotherapeutics worldwide, with AAV at the forefront. This rapid growth is constantly challenging CMC approaches, from manufacturing through release ...

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 ...

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 ...

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 ...

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 ...

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 ...

USP's nitrosamine testing project with Vietnam NIDQC advancing global drug safety: Vietnam Thursday, April 9, 2026, 17:00 Hrs [IST] A groundbreaking three-year collaborative pilot ...

The FDA has issued an alert to healthcare professionals of a change in heparin manufacturing that is expected to decrease the drug?s potency. The FDA has issued an alert to healthcare professionals of ...

The U.S. Pharmacopeial Convention has released new rules designed to standardize the format, appearance, content and language found on medication labels for patient safety. Studies have found shown 46 ...

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 ...