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Unpacking Sweden’s regulatory frameworks: Who approves medicinal products and medical devices, and how are product categories determined?

25/11/2024

We are pleased to announce that our latest article, "Pharma & Medical Device Regulation 2025 – Sweden”, has been published on Lexology Panoramic, with contributions from Malin von Heideken, Sofia Falkner, and Timothy Mjällby.

You can read the chapter by clicking on the following link: Compare - Panoramic - Lexology

Lexology Panoramic (formerly Getting the Deal Through) offers a comprehensive view of how laws and regulations differ across jurisdictions. This market-leading cross-jurisdictional comparison tool features insights from leading practitioners around the globe.

Team involved

Malin von Heideken_3

Malin von Heideken

Partner

malin.vonheideken@hammarskiold.se

+46 702 38 47 00

Sofia Falkner_3

Sofia Falkner

Partner

sofia.falkner@hammarskiold.se

+46 708 94 40 43

Timothy Mjällby_2

Timothy Mjällby

Associate

timothy.mjallby@hammarskiold.se

+46 708 94 45 79

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