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Enhancing Medical Product Safety Through Regulatory Innovations

This organization focuses on ensuring medical product safety through efficacy assessments, regulations, and innovative approaches. With a dedicated team of professionals and expertise in pharmacovigilance, cosmetics control, and clinical trials, the organization aims to create a secure healthcare environment. Services include licensing, information management, and supervision of medicinal products to guarantee quality and safety for consumers. Through collaboration with external relations and the pharmaceutical industry, the organization aims to drive innovation while ensuring regulatory compliance.

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Enhancing Medical Product Safety Through Regulatory Innovations

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  1. Director General Bengt Wittgren (Act) InternalAudit Advisory Council Administration Enrique Arias DG Staff Eva Andersson Assistant Director of Administration Staff DG Staff Planning, Budget and Finance Information Technology Registration and Information Management Development Gert Ragnarsson (Act) Licensing Thomas Uhlin (Act) Usage Anders Carlsten Supervision Karin Hååg Facilities and Services ScientificExpertise Efficacy and Safety 1 Medical Devices Medical Information Legal Affairs External Relations and Innovation Support Efficacy and Safety 2 Cosmetics Use of Medical Products Efficacy and Safety 3 Pharmacovigilance Officials Medicines Control Laboratory Supervision of MedicinalProducts and Narcotics Human Resources Thomas Ekvall Efficacy and Safety 4 Swedish Poisons Information Centre Communications Pharmaceutics and Biotechnology DrugInspectorate Human Resources Product Information Pharmacies and OTC Retailing Centre for Rational Use of Medicines Madeleine Wallding RegulatoryAdministation Clinical Trials and Special Permissions HerbalMedicinalProducts

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