Swiss-exit, Turkey-exit, BREXIT and Medical Device Regulation
Articles filtered by tag
EU Medical Devices Regulation: 26 May 2021
Pegah Kiani, Director of Quality Assurance and Medical Devices, highlights what you need to know.
Regulations & Guidance: Clinical Trials
Q1’s Industry Insights round up all the latest regulatory news
MHRA Post-Transition Period Information
All the information you need on the BREXIT transition direct from our Regulatory Team
MHRA Submissions – The UK submissions portal from 01 January 2021
Find out about the MHRA Submissions Portal by talking to our team.
Clinical Trials News from around the Globe
All the latest regulatory updates compiled for you by S-cubed.
Clinical Development Practices & Regulations
Our latest Industry Update for Q2 covers the latest regulatory information around COVID-19 and much more.
Clinical Trial Regulation, ICH E6(R2) & Brexit
Our first Industry Update of 2020 focuses on Clinical Trial Regulation, Brexit and the latest from FDA & EMA.
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.
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.