Hammarskiöld’s Malin von Heideken, Sofia Falkner, Timothy Mjällby and Ida Timan have contributed the Sweden chapter to Lexology Panoramic: Pharma & Medical Device Regulation 2026.
The chapter provides an overview of the Swedish regulatory framework for pharmaceuticals and medical devices, covering key areas including product classification, clinical practice, marketing authorisations, advertising and promotion, pricing and reimbursement, and other key regulatory considerations.
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The full Sweden chapter is available in English and can be read via the Lexology link: Compare - Panoramic - Lexology or as a PDF Sweden - Pharma & Medical Device Regulation.



























































