President Trump wants pharmaceutical production to return to the United States. A shuttered factory in Louisiana shows how ...
The track by which API manufacturing processes are prepared for commercial use is comparable to overlapping integrative process evaluations at commercial scale. This ensures the process is ...
As the prospect of import tariffs and drug price reform marshals billions of biopharma investment dollars into the U.S., the ...
Because scope 3 covers the entire value chain, pharma scientists should integrate sustainability into R&D, manufacturing, and ...
Some of the most expensive drugs currently in use are gene therapies to treat specific diseases, and their high cost limits ...
HENGDIAN, China, Aug. 27, 2025 (GLOBE NEWSWIRE) -- Hengdian Group’s pharmaceutical arm Apeloa is using Flow Chemistry, a safer and more environmentally-friendly manufacturing approach than traditional ...
Granulation is a critical unit operation in pharmaceutical manufacturing, where fine powders are agglomerated into granules to improve flow properties, uniformity, and compaction performance. The ...
The White House on May 5, 2025 issued an executive order requiring the US Food and Drug Administration to find ways to facilitate the opening of new drug manufacturing sites in the United States while ...
Ensuring the safety and quality of pharmaceuticals, such as blood products, vaccines, recombinant proteins, and monoclonal antibodies, is essential. Endotoxins act as a hidden ‘time bomb’ in these ...
―New State-of-the-Art Facilities Will Triple the Company’s Space and Greatly Increase Its Manufacturing Capacity for APIs for Clinical Trial Materials and Ultimately Commercial Production― EUGENE, Ore ...
Environmental contamination control is a crucial aspect of sterile pharmaceutical manufacturing, and risk management is needed to guarantee that the necessary control procedures are in place. The risk ...
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