Trial complications latest issue to prompt Brexit concerns

28 July 2020
brexit_big

GBA Group Pharma, a European service provider for pharma and biotech companies, has warned of risks to drugmakers’ clinical trial plans caused by Brexit.

As recently confirmed by a technical note from the European Commission and the European regulatory authorities, healthcare companies could meet significant business difficulties when running European Union (EU) trials through UK-based qualified persons, as of January 1, 2021.

With no extension of the transition period requested by the UK as of July 1 this year, it will be treated as a third country by the EU regulatory authorities from January 2021 onwards.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK

Today's issue

Company Spotlight





More Features in Pharmaceutical