06.07.2026

CIRS study on authorisation times for human medicinal products with new active substances confirms Swissmedic’s competitiveness internationally

International authorisation times for human medicinal products with new active substances during the period 2016–2025

01.07.2026

TPLRO, TPLO: Update of annexes

Update of the TPLRO and TPLO annexes

01.07.2026

Patient information and Information for healthcare professionals for human medicinal products: Change to the templates

Change to the Patient information and Information for healthcare professionals templates

01.07.2026

Fassung 12.3 der Europäischen Pharmakopöe in Kraft

Der Institutsrat hat die Fassung 12.3 der Europäischen Pharmakopöe auf den 1. Juli 2026 in Kraft gesetzt

01.07.2026

Safety Update – product information updates

Important new safety information in professional information – overview July 2026

30.06.2026

Cross-agency targeted campaign "Peptides 2026"

Swissmedic and SSI warn of the health risks associated with illegally imported peptides and conduct a joint campaign with FOCBS

In focus

Fillerbehandlungen

Filler Treatments

The video highlights the risks of not getting filler treatment from a specialist and explains how to reduce these risks. 

Contact for members of the public

Do you have any questions about a particular medicine or a general question about Swissmedic? We’ll be glad to be of assistance. 

Just send an e-mail to questions@swissmedic.ch or use our contact form. Thank you.

Direct links


Stay up to date


Reporting undesirable effects and incidents

Medicines


Medical devices

Swiss Public Assessment Report (SwissPAR)

SwissPAR

Summary report on authorisation

Featured


Swissmedic video portrait

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!

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01.07.2026

Introduction of the obligation to register in swissdamed

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.

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What are the tasks of Swissmedic in the area of medical devices?

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.

Medical devices: List of Field Safety Corrective Actions (FSCA) and recalls

Swissmedic monitors all safety measures and recalls for medical devices that are manufactured or marketed in Switzerland.


Swissmedic, Swiss Agency for Therapeutic Products

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Swissmedic – for therapeutic products you can trust

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.

For further information...
https://www.swissmedic.ch/content/swissmedic/en/home.html