As 25 May 2018 is nearly upon us, here is a reminder of its impact on Life Sciences and Medical Device businesses. Read more (PDF document). 

S&B's Gustaf Duhs brings you up to speed on changes to Medical Device Regulations in the May issue of Pharmaceutical Market Europe. Read more (registration required)

Charlotte Tillett and Camille Arnold share their expertise in their recent co-authored article published in Pharmaphorum. Read more

The Transparency Regulation (Regulation EC 1049/2001, the “Regulation”) governs public access to European Parliament, Council and Commission documents. Although it came into force in 2001, it is back in the news due to the General Court rulings on three appeals against the European Medicines Agency’s (“EMA”) disclosure of documents provided as part of Marketing Authorisation applications. Read more