Cell therapy manufacturing is uniquely vulnerable to contamination, variability, and operational burden because the product - ...
Dublin, Jan. 14, 2026 (GLOBE NEWSWIRE) -- The "New EU (European Union) GMP (Good Manufacturing Practice) Annex 1: Compliant Aseptic Operations Training Course (May 19th - May 21st, 2026)" training has ...
The collaboration integrates Demeetra’s CleanCut CHO platforms and cell line services with NorthX Biologics’ GMP ...
In drug manufacturing, aseptic filling is the crucial final step in advancing biologics candidates into the clinic. Whether drug manufacturers outsource the process to a CDMO or bring the filling ...
In August 2022, the European Commission published a revision to Annex 1 “Manufacture of Sterile Medicinal Products” in EudraLex - Volume 4 - Good Manufacturing Practice (GMP) guidelines that will ...
Upperton has submitted an application to the UK’s Medicines and Healthcare Products Regulatory Agency for approval of its new sterile manufacturing facility.
VelQuest SmartLab EM Improves Efficiency, Cuts Errors in Aseptic Process Monitoring HOPKINTON, Mass., July 27, 2011 /PRNewswire/ -- VelQuest Corporation, world leader in lab execution systems for the ...
ROCKVILLE, Md.--(BUSINESS WIRE)--ABL, Inc. (ABL), a leading contract research, development and biomanufacturing organization to the biopharmaceutical industry worldwide, is proud to announce the ...
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