In our weekly expert view piece Dr Nick Meyers, programme director at Boyd Consultants examines the implications what the regulatory and legislative landscape in the biopharmaceutical industry could look like post-Brexit.
In this article, I aim to explore, without any bias in favour either of remaining in or leaving the EU, some of the practical consequences for biopharmaceutical companies undertaking research and development with a view to commercialising their products, of a potential exit from the European Union; a so-called ‘Brexit’ following the June 23 referendum i.e., what changes might be required, in terms of the way we work on a daily basis.
It is of course formally possible that a vote to leave could trigger a counter proposal from the EU, involving additional concessions, aimed at persuading Britain to remain a member, which would likely require a second referendum to either reverse or reiterate the outcome of the first, in the light of any new deal for the UK.
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