Quality & Compliance

Pharma companies have been raising awareness for years, but patients continue to buy counterfeit medicines online.

At SGS, we are performing in vitro testing to assess the chemical potential for sensitization.

How to manufacture your API in the right quantity, at the right cost, and in the right time frame.

What are the most important things to consider when filing an IND? This infographic, sponsored by Regis, sets out the five key steps to success.

GDUFA fees for 2020 have been decided – and include a significant drop in the fees for finished dosage facilities.

Fail to Prepare? Prepare to Fail…

Viral contamination can shut down a plant for months – affecting manufacturing, causing business disruption and threatening supply and patient safety.

By simulating processes in a digital twin of a facility, changes can be safely tested before application in the real world.

Qualitative risk assessments are a great way to approach quality management and train your operators at the same time.

As a leading partner and supplier to the industry, MilliporeSigma continues to strengthen and enhance its supply chain capabilities.