Gruppo FarmaImpresa at the Top of European Quality: Maximum Safety for Gynecologic Well-Being The EU Regulation 2017/745 (MDR) is Europe’s most stringent framework for manufacturing and marketing medical devices. It raises the bar on safety, quality, and traceability, introducing far stricter requirements than previous directives. For Gruppo FarmaImpresa, obtaining MDR certification for the Class IIb…
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…
Registration of Class IIa Medical Device for Gastroesophageal Reflux at the Department of Health in Hanoi, Vietnam The Department of Health in Hanoi, Vietnam officially registered our Class IIa medical device. Additionally, it’s important to note that the device holds an MDD certificate extension. The device is an oral emulsion composed of key actives: low…