The PBL manufacturing facility at Porton Down, Wiltshire, UK is licensed by the MHRA under the Human Medicines Regulations 2012 (as amended) (SI 2012/1916) Manufacturer’s Licence No. MIA 44403 and The Medicines for Human Use (Clinical Trials) Regulations 2004 Manufacturer’s Licence No. MIA (IMP) 4403.
In December 2019, following our most recent inspection (October 2019), the MHRA confirmed that the operations are in general compliance with the principles and guidelines of good manufacturing practice as laid down in Commission Directive 2003/94/EC.
This part of the site is currently under construction.