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Friday, December 03, 2021 3:50:15 AM
Has been inspected under the national inspection programme in connection with manufacturing authorisation no. UK MIA(IMP) 32390 in accordance with Part 6 of The Medicines for Human Use (Clinical Trials) Regulations 2004 (SI 2004/1031)
From the knowledge gained during inspection of this manufacturer, the latest of which was conducted on 30/11/2021, it is considered that it complies with
The principles and guidelines of Good Manufacturing Practice laid down in Regulation B17 of the Human Medicines Regulations 2012 (as amended)
72 Hours from inspection to certification ...
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