Visit Us at CPhI Milano

Visit Us at CPhI Worldwide Milano – Stand 14D69 We are excited to announce that from October 8 to 10, we will be at CPhI Milano at Fiera Milano, Hall 14, Stand 14D69. We look forward to welcoming you to our stand and showing you what we have in store.   đź“Ť Where to Find…

MDR: extension of the transition period has been accepted!

MDR extension: accepted proposal to amend European Regulation 2017/745 (MDR) The proposal to amend European Regulation 2017/745 MDR and European Regulation 2017/746 IVDR, announced on December 9 during the EPSCO meeting, has been approved. The main objective of European Regulation 2017/745 MDR (Medical Device Regulation) is to “establish a robust, transparent, predictable and sustainable regulatory…

Gruppo FarmaImpresa receives first MDR certifications

Gruppo FarmaImpresa is among the first Italian companies to obtain MDR certifications for some of its substance-based medical devices As a reminder, the new Regulation (EU) 2017/745 or MDR (Medical Device Regulation) is the European medical device regulation that defines regulations and constraints that all manufacturers and distributors must comply with in order to place…