With a post-transition Brexit looming on the horizon, the Medicines and Healthcare products Regulatory Agency (MHRA) have recently published guidelines relating to new rules dealing with, amongst other things, medical devices and medicines, which need to be complied with from 1 January 2021. In this note, we unpack some of the main points included in the guidance relating to the regulation of existing centrally (EU) authorised medicines and the importing of medicines into the UK.
During...
September 30, 2020
7 min read