Curcuma Longa: Regulations and Safety of High Curcumin Extracts in Europe – Recent Developments and Prospects In recent months, concerns have arisen regarding the use of Curcuma extracts and their suitability for indications and prescriptions. The AME Drugs Commission (Association of Endocrinologist Physicians) has examined this issue and determined that the use of dietary supplements…
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…
The new Regulation (EU) 2017/745 or MDR is the European medical device regulation that defines regulations and constraints that all manufacturers and distributors must comply with in order to place a medical device on the European market. The new Regulation complements and replaces the previous Directives 90/385/EEC and 93/42/EEC, providing more stringent requirements and measures…