Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic)
clinical trial master file
Medicines verification system goes live across EU
Medicines verification system goes live across EU to better protect patients from falsified medicines
EMA now operating from Amsterdam
EMA move to AMSTERDAM has been realized on 11 March 2019
New Swissmedic application forms for operating licences
Swissmedic has prepared new forms for manufacturing licenses in line with European EudraGMDP database
Stability Studies Needed to Define Transport Conditions of Sensitive Products
Many pharmaceutical or biotechnological products require transport using temperature controlled systems to keep …
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