BioCina Pty Ltd., a global end-to-end Contract Development and Manufacturing Organisation (CDMO) announced it has initiated a ...
As the demand for biologics accelerates, biopharma companies are under pressure to expand sterile manufacturing capacity ...
Why is aseptic processing important in pharmaceutical manufacturing? The manufacturing of both sterile drugs and biological products can be achieved through terminal sterilization or aseptic ...
LEE — In the past several years, Berkshire Sterile Manufacturing has been significantly increasing its capabilities and expanding its potential market. This has included the development of two new ...
-Adds BFS platform technology to provide large-scale production capacity for sterile drug dosage forms, including injectables, ophthalmics and inhalation Amneal will install dedicated manufacturing ...
Purpose-built 11,000 sq. ft. site with 2,000 sq. ft. cleanroom brings modular, high-yield sterile fill-finish to clinical and early-phase commercial programs Sevenoaks, UK — [January 07, 2026] — ...
Upperton Pharma Solutions submits MHRA application for a new Annex 1–compliant sterile manufacturing facility, expanding clinical-scale CDMO capacity for biotech and pharma companies.
1. In a story on respect for sterile processing: Operating room teams should treat sterile processing staff with respect to achieve optimal patient safety and employee satisfaction outcomes, according ...
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