Switzerland continues to reinforce its regulatory oversight of medical devices as part of its commitment to maintaining high standards for patient safety and product quality. In recent regulatory updates, the Swiss authority has emphasised the importance of robust market surveillance and regulatory compliance for manufacturers placing medical devices on the Swiss market. The country’s regulator, Swissmedic, plays a central role in ensuring that medical technologies available

Swissmedic released an important amendment to its guidance document on Good Manufacturing Practice (GMP) compliance for foreign...

Swissmedic, the Swiss regulatory authority for therapeutic products, has introduced updates to its guidance documents for the Fast-track...

Albania: Amendments proposed to ‘Law on Medical Devices’ EU: New MDCG documents on Notified Bodies, the person responsible for regulatory...