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Comprehensive Regulatory Administration for Medicinal Products

Streamlined advisory council enhancing safety and efficiency in medical device and cosmetic use. Expert supervision and licensing services ensuring efficacy and safety standards. Effective information management for pharmaceutical and biotechnology sectors.

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Comprehensive Regulatory Administration for Medicinal Products

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  1. Advisory Council Administration Enrique Arias Director General Christina Åkerman Assistant Director of Administration Staff InternalAudit Deputy DG Bengt Wittgren Planning, Budget and Finance Information Technology Communications and Head of Legal Affairs Registration and Information Management Facilities and Services Development Bengt Wittgren Licensing Thomas Uhlin Usage Anders Carlsten Supervision Karin Hååg Legal Affairs ScientificExpertise Efficacy and Safety 1 Medical Devices Medical Information External Relations and Innovation Support Efficacy and Safety 2 Cosmetics Use of Medical Products HumanResources Thomas Ekvall Efficacy and Safety 3 Pharmacovigilance OfficialMedicines Control Laboratory Supervision of MedicinalProducts and Narcotics Efficacy and Safety 4 Swedish Poisons Information Centre Human Resources Pharmaceutics and Biotechnology DrugInspectorate Industry and Hospital Product Information Pharmacies and OTC Retailing Centre for Rational Use of Medicines Madeleine Wallding Regulatory Administration Clinical Trials and Special Permissions In force from 1 September 2013 HerbalMedicinalProducts

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