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Will use advanced VHP isolation technology and carry out GMP fill-finish of sterile drug products for biologics and small molecules.
January 16, 2024
By: Anthony Vecchione
Upperton Pharma Solutions, a contract development and manufacturing organization (CDMO), reported a £5 million investment to expand operations into small-scale sterile fill-finish. After completion of a new 50,000 sq.-ft. GMP facility in 2023, the UK-based company will expand its Trent Gateway site to include sterile capabilities with a purpose-built facility designed specifically in line with the revised EU GMP Annex-1 regulations. Construction of the facility will begin this February and...
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