Nordic Regulatory Consultants

Regulatory Affairs consultant in the pharmaceutical, medical device and related areas.

Owner

Svenska institutet för standarder, SIS

Member TC355 (Quality and risk handling management)

Läkemedelsakademin (Swedish Academy of Pharmaceutical Sciences)

Lecturer

Swedish Academy of Pharmaceutical Sciences, Medical Device Section

Vice Chairman Of The Board, retired

Swedish Academy of Pharmaceutical Sciences - Medical Device Section

Chairman of Board

Swedish Academy of Pharmaceutical Sciences - Special Interest Group Medical Devices

Chairman

Uppsala Riksteaterförening

Board member

Swedish Academy of Pharmaceutical Sciences (Apotekarsocieteten)

Convener TC340/WG1 (Clinical Investigation)

Member TC336 (Ophthalmic Implants)

Member TC340 (Biological Safety)

ISO International Organization for Standardization

Took vivid part in the writing of the new ISO 14155 standard on Good Clinical Practice for Medical Devices

Member and Editing Committee member ISO TC 192/WG4  (Clinical Investigation)

Member ISO TC 172/SC 7/WG 9 (Contact Lenses)

Member ISO TC172/SC7/WG7 (Ophthalmic Implants)

Former Vice Chairman Of The Board på Apotekarsocieteten, Medical Device Section

Regulatory expertise on pharmaceuticals, medical devices and related product types for more than 45 years. 
Open to new industrial board and advisory committe assignments! 
Specialties: Regulatory Affairs for pharmaceuticals, medical devices, natural remedies, cosmetics etc. Borderline product classification is a speciality!

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