· 1 min read
Have you lost touch of all the essential regulatory updates due to COVID-19?
Our detailed regulatory update section has you covered. This includes all the latest U.S. and European pharma and medical device regulatory news, including ICH, updates on the EU MDR, Brexit and more. Regulatory affairs expert Marinka Tellier also reviews the U.S. regulatory preparedness in facing the COVID-19 pandemic.
We also welcome Emma Ewins to the pharma team in a virtual interview, and Na Ry Woo, a Korean Ministry of Food and Drug Safety (MFDS) Scientific Reviewer, shares her current experiences on her one-year regulatory program with Amarex Clinical Research.