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Scandinavian Regulatory Services


Who we are


We are a team of pharmaceutical and medical device regulatory specialists with extensive experience from all different aspects of regulatory affairs covering a wide range of products. All consultants have long-term experience in the field of regulatory affairs: leading functions in the international pharmaceutical and medical device, as well as IVD industry, regulatory manager positions in international affiliate companies, and positions within regulatory agencies.

SRS has 10 employees and about 20 specialized consultants in various fields.


The company has two major competence areas:


Pharmaceutical Regulatory Affairs where Lars Janson is the regulatory expert and Medical Device Regulatory Affairs where Ann-Cathrin Jareman is the regulatory expert.
Ann-Cathrin Jareman Ann-Cathrin Jareman
Managing Director and Medical Device Regulatory Expert (M.Sc.)

Ann-Cathrin has 20 years experience from working mainly with CE-marking, FDA-clearance, registration and quality systems for medical devices, including IVDs.
Lars
                      Jansson Lars Jansson
Business Development, Senior Expert/Co-founder SDS (M.Sc.)

Lars has more than 30 years experience in regulatory affairs and drug development from international pharmaceutical companies and regulatory authorities.

ABOUT US

REGULATORY SERVICES

Compliance

MARKET ACCESS

BROKER ACTIVITIES

Creator's notes