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This submission follows the successful completion of aseptic process simulation validation batches executed under the requirements of the revised EU GMP Annex 1 requirements.
March 5, 2026
By: Charlie Sternberg
Associate Editor
Upperton has submitted an application to the UK’s Medicines and Healthcare Products Regulatory Agency for approval of its new 7,000‑square‑foot sterile manufacturing facility in Nottingham. The filing follows completion of aseptic process simulation validation batches performed under the EU’s updated GMP Annex 1 standards. The site, built to current Eudralex Volume 4 Annex 1 requirements, expands Upperton’s footprint alongside its existing 50,000‑square‑foot development and manufacturing faci...
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