Posted by Claus Andersen, Partner
End of Brexit transition period – what now for medicines and medical devices?
With the end of the Brexit transition period fast approaching it is becoming more and more urgent for businesses in the medical sector to prepare for the transition period coming to an end. It is a sector, where many of the rules stem from EU regulation, which makes it even more important for businesses to prepare.
To this end the Medicines and Healthcare products Regulatory Agency (MHRA) has produced a set of guidance notes, which explain the rules in relation to:
- Clinical Trials
- Devices
- Licensing
- Importing and exporting
- IT systems
- Pharmacovigilance and
- Paediatrics
The rules are quite complex and businesses this sector should consider how the end of the transition period may affect them and plan for the effects. The guidance can be found here.
If you have any questions about how Brexit may impact your business, please feel free to contact Claus Andersen on:`
020 7842 1462 Email us
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