Ottawa, Nov. 04, 2025 (GLOBE NEWSWIRE) -- The sterile drug product testing market is set to witness robust growth from 2024 to 2034, fueled by the expanding production of biologics and injectable ...

Microorganism lethality requirements for process validation must always be balanced with the need to protect product integrity and patient safety. Submitted: Feb. 9, 2015. Accepted: May 29, 2015.

In April of this year, the Food and Drug Administration (FDA) issued an alert about products shipped from NuVision Pharmacy of Dallas because of poor sterile production practices. In April of this ...

Lowlite Investments Inc, doing business as Olympia Pharmacy in Orlando, Florida, has initiated a voluntary recall of all unexpired sterile drug products compounded by the pharmacy because of a lack of ...

TOPEKA (KSNT) – Medical supplies distributed nationwide in the U.S. are being recalled as the products may not be sterile due ...

All nonexpired sterile drug products from Unique Pharmaceuticals Ltd of Temple, Texas, are being recalled because of a lack of sterility assurance, the US Food and Drug Administration (FDA) said today ...

The U.S. Food and Drug Administration is alerting hospitals, health care providers, veterinarians, and patients of a voluntary recall of certain human and veterinary products produced and distributed ...

DETROIT (WWJ) - There's a recall involving sterile products used to inject medication. The FDA says a company called Specialty Compounding LLC., will voluntarily recall its full line of sterile ...

Delegates will learn about the GMP requirements for sterile products and areas likely to be looked at during Regulatory Inspection. The course provides delegates with an increased knowledge of the GMP ...

Axia Pharmaceutical is recalling all lots of its sterile drug products because it says it cannot guarantee they are sterile. Drugs that are intended to be sterile but are not could cause ...