Medical Device Regulation: Toward Efficiency and Innovation

Navigating the Future of Medical Devices: A Deep Dive into the European Commission’s MDR Revision and Industry Proposals for a More Efficient and Innovative Landscape The European Commission has officially announced the launch of the Medical Device Regulation (MDR) revision, a welcome development for the industry. This initiative, communicated by European Commissioner for Health, Olivér…

Oral Emulsion for the Treatment of Severe GERD

Medical device with Hyaluronic Acid, Magnesium Alginate, and Myrrh: intense and lasting relief against gastroesophageal reflux Starting from 2025, we have officially registered our Class IIa medical device for the treatment of severe gastroesophageal reflux disease (GERD) with the Ministry of Health and Prevention of the United Arab Emirates (UAE). Severe GERD: a significant impact…

GFI obtains registration on the EUDAMED portal

EUDAMED: Gruppo FarmaImpresa achieves registration as a Manufacturer and Producer of Procedural Systems/Kits In recent years, the European Union has shown a growing concern for the safety and effectiveness of medical devices used within the European market. To enhance monitoring and ensure stricter control of these devices, the European Commission has developed EUDAMED (European Database…