Specialist data for complementary medicines in the notification procedure (Chapter 7 KPTPO) in the Swissmedic Portal for marketing authorisation holders
Swissmedic publishes the new «Schweizerische Gute Praxis der Materiovigilance in der In-vitro-Diagnostik» (GPMV-IVD). This guideline is intended to support professionals using in vitro diagnostic medical devices (IVDs) for medical purposes, as well as persons responsible for the implementation of medical device vigilance in the field of in vitro diagnostics
Swissmedic monitors all therapeutic products on the market in Switzerland. Our independent experts ensure the therapeutic products you and your loved ones need are effective, safe and of the highest quality.
What is a medicinal product?
Did you know that tea can also be a medicinal product? But what exactly constitutes a medicinal product and how does it differ from other products? You will find answers to these and other questions in this video.
Delimitation questions in human health
In order for a product to be sold, it must comply with the relevant legal regulations. However, it’s not often immediately apparent which product group it belongs to. In this video, we explain what different categories there are, and when a product is really a therapeutic product – and when it is not!
The obligation to register products for medical devices, in vitro diagnostic medical devices, as well as systems and procedure packs in swissdamed has applied since 1 July 2026 (communication.
The factsheet “Economic operators” (PDF, 1 MB, 01.05.2026) and the “swissdamed” section of the website have been updated.
Further information on the EU Regulations and their implementation in Switzerland is available under: Legal framework.
What is a medical device? How do medical devices come onto the market? How do you recognise a medical device? Based on examples, our videos answer these and a number of other questions.
Swissmedic is the Swiss authority responsible for the authorisation and supervision of therapeutic products. Swissmedic's activities are based on the Law on Therapeutic Products.
