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FDA

Medical Device Reprocessing Testing

Looking for medical device testing? On March 12, 2015, the US Food and Drug Administration released a final guidance for medical device reprocessing entitled "Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling”  This guidance was...

Medical Device Reprocessing Testing

21st Century Cures Act

The FDA is continually working to improve patient outcomes by including patients as well as their comfort and safety in the development of new drugs, biologics, and medical devices. A relatively new law, the 21st Century Cures Act, was designed as a way to bring...

FDA Compliance in Veterinary Medicine Testing

FDA compliance in veterinary medicine testing is not only a regulatory requirement but also a benchmark for quality and safety in animal health products. Ensuring the safety and efficacy of veterinary drugs, devices, and food additives is a top priority that...

Veterinary Medicine Research and Development Testing

Biosimilars: A Comprehensive Overview

What are Biosimilars? Biosimilars are biologic medical products that are highly similar to an already approved reference biologic drug, also known as the originator or innovator biologic. These reference drugs are typically complex, large-molecule drugs derived...

image showing biosimilar drugs in a pharmaceutical setting

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