All the information you need on the BREXIT transition direct from our Regulatory Team
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MHRA Submissions – The UK submissions portal from 01 January 2021
Find out about the MHRA Submissions Portal by talking to our team.
Latest News in Clinical Development Practices and Regulations
Our latest Industry Insights focuses on Brexit and news from the regulators around the globe.
Brexit, EMA, FDA & Global Regulatory News
Our first Industry Insights of 2019 focuses on the latest regulatory developments and Brexit.
Regulatory Affairs & Quality Assurance: Copenhagen
Jakob Sandersen reports on the exciting developments at Pharmaceutical Services ApS over the last 15 months.
SME Day at EMA – Part 3
The final report on the SME Day at EMA focuses on the Committee for Advanced Therapies, new Medical Devices Regulation and a Brexit update.
Brexit Update, Clinical Trial Data Sharing, & more
Our latest industry update covers news about Brexit, from FDA, EMA and more.
The Impact of Brexit on Pharmaceuticals in the UK – UPDATE
Stephen Thompson, our regulatory affairs Director, writes about the latest Brexit news.
Brexit, access to medicines, data & data sharing
Our latest update from the industry reflects the ongoing uncertainty around BREXIT.