Medicines manufactured by the National Health Service are subject to requirements of the Human Medicines Regulations 2012/1916. As such the manufacturer must be licensed by the Medicines and Healthcare products Regulatory Agency (MHRA) and must comply with specified quality standards. The licence provides for stipulated processes to be conducted. There is a public register of all United Kingdom licensed manufacturers of medicines for human use on the Government services website GOV.UK at:
The MHRA does not hold data on what medicines the NHS manufactures.