In this Pharma Matters Q&A, Amina Rahmoune of Nelson Labs evaluates and compares sterility testing in cleanrooms and isolators.

An interview with Gilberto Dalmaso, discussing the different grades of pharmaceutical cleanrooms and the production of high-level compounds under aseptic conditions. Please give an overview of ...

Please define the meaning of “risk” from the perspective of environmental monitoring. Risk assessment consists of the identification of hazards and the analysis and evaluation of risks associated with ...

DUBLIN--(BUSINESS WIRE)--The "Global Sterility Testing Market, 2017 to 2025" report has been added to Research and Markets' offering. The global Sterility Testing market was valued at US$ 548.2 Mn in ...

DUBLIN--(BUSINESS WIRE)--The "Pharmaceutical Sterility Testing Global Market Report 2020-30: Covid 19 Impact and Recovery" report has been added to ResearchAndMarkets.com's offering. The global ...

As demands for aseptic manufacturing increase, partnerships among solutions providers will become key to ensuring safe, ...

To assure patient safety, biologics developers and manufacturers must carefully consider where contaminants could be introduced to the drug substances (DSs) or drug products (DPs) at all stages of the ...

A fully automated aseptic fill-finish platform delivers greater speed, flexibility, and quality for the manufacturing of ...

(MENAFN- GlobeNewsWire - Nasdaq) Robust expansion currently defines the landscape as major players like Eli Lilly and Merck aggressively fund new manufacturing facilities. Concurrently, the industry ...