If a “worst-case scenario” was actually to happen, Swiss manufacturers will have to meet third country requirements.
MDR Update: Notified Body designations and first MDR CE Certificate
European Commission announce first four notified body designations and first CE certificate awarded under Medical Device Regulation 2017/745/EU.
Switzerland is aligning the medical devices legislation to the future EU Regulations
Switzerland aligns with EU medical device legislation to make crucial improvements to patient and consumer safety. The country expects to be aligned by 2020.
Registering Cosmetic Products in Spain
What is the process of registering cosmetic products in the Spanish market.
Switzerland harmonizes Cosmetics Regulation with EU’s
Under Project LARGO, Switzerland has overhauled its food and consumer product regulations, harmonizing them with current EU laws and standards.