Brexit impact on UK pharma industry a moveable feast, industry experts tell CPHI Discover

The UK’s withdrawal from the European Union has meant the pharmaceutical industry has had to adapt to some monumental changes in terms of research, regulatory affairs, and trade. In this CPHI Webinar, three industry experts discussed what the future may hold for UK pharma in a post-Brexit world

Framing the discussion in the session, Beyond Brexit – The Future of British Pharma, Virginia Acha, Associate Vice President & Global Lead, Global Regulatory Policy, MSD said much has been learned since the first days of Brexit.

“Critically, we were talking about and expecting Brexit as an event but it’s not an event, it’s a process and going way beyond the actual Brexit date itself and this is why we need to be as focused now as we ever were about how we reposition the UK in the international landscape,” she told the audience.

She said that whereas in the first years since the Brexit referendum, the focus used to be on what the country was leaving, “now the direction of our work needs to be towards where we’re going, what ambitions do we have, both in terms of regulatory policy setting and more generally, for healthcare and patients in the UK.”

“We also need to be aware that while we were busy in the UK and Europe managing the Brexit process, regulatory science has moved on and some of the examples around real world evidence and genomics really show where that pressure has been and where the opportunities are now to reposition,” Ms Acha said.

Peter Gough, Vice President, Pharmaceutical Services at NSF International said that since Brexit, the UK had chosen to place itself as a third country outside all the European institutions including the EU, the customs union and the EEA: “We’re sitting there in splendid isolation, outside everything, which provides opportunities and challenges.”

He told the webinar it was important to note that the Northern Ireland protocol effectively means that Northern Ireland remains in the European system and therefore most pharmaceutical regulatory changes only apply to Great Britain.

“From next year, we’re going to face the challenge of how do we actually get product from Great Britain into Northern Ireland because effectively, that will be exporting to the EU and will require retesting om importation and re-QP certification,” he said.

Providing a clinical research perspective, Angela Macfarlane, Senior Market Development Director UK & Ireland, IQVIA said she was “cautiously optimistic” that there would be a fresh start for global pharma investment in the UK, listing initiatives such as the transformation of the UK clinical research ecosystem, realising the promise of precision medicine via the UK’s genomics strategy, accelerating license and HTA approvals and the Innovative Medicines Fund.

Ms Macfarlane said the global coronavirus pandemic had been a catalyst for life science cooperation and that was one of the real defining features of how UK industry, the country’s National Health Service, government and regulatory agencies really came together to work at pace and scale to discover COVID treatments and vaccines.

“That earning has now been embedded into policy; collaboration is going to be the key to continuing to develop UK life sciences on a global stage,” she added.

She cited National Institute for Health Research data which showed end to end approval times at UK regulator, the Medicines and Healthcare products Regulatory Agency (MHRA), including the time for applicants to respond, had shortened from an average 8-8.5 days depending on the study type, compared to more than 80 days pre-COVID.

This webinar will be available on demand from 31 May. In the meantime, for details on how to register for this ongoing virtual event, head to the CPHI Discover website