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.   📍 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…