New EU Rules for Food Supplements: What You Need to Know

A crucial update for the nutraceutical sector The food supplements sector is constantly evolving and requires continuous updates from manufacturers, distributors, and healthcare professionals. One of the main sources of regulatory change in Europe is the application of Article 8 of Directive 2002/46/EC, which allows the European Commission to take preventive action on ingredients considered…

The importance of certifying medical devices under MDR

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…