The Implications of Brexit on the Pharmaceutical, Medical Devices & Clinical Trials Sectors
Acorn Regulatory has published a whitepaper looking at the potential implications of Brexit on a number of healthcare sectors. The document looks at the impact of the UK’s decision to leave the EU on institutions such as the EMA. It also focuses on the EU’s Medical Device Directive and the regulations surrounding clinical trials.
Speaking at the launch of the document, Managing Director of Acorn Regulatory Dr. Gemma Robinson said “There is now great uncertainty for the industry sectors that we cover. Questions about appropriate regulatory strategies, potential differences in regulatory frameworks, the relocation of the European Medicines Agency, loss of a powerful national competent authority all hang in doubt. This briefing document aims to throw light on what Acorn Regulatory sectoral experts know now and what they believe will happen”.
This is the first document in a series of whitepapers on the ‘Brexit’ issue.
Read the whitepaper on the implications of Brexit by completing the details below:
Since the publication of this first Acorn Regulatory Brexit whitepaper, we have continued to publish further whitepaper. You can download and read them by clicking the links below.
