About us

Scandinavian Regulatory Services AB (SRS) is a Swedish consultancy company founded in 1992. We offer regulatory and quality expertise and services to the pharmaceutical, medical device and associated industries.

SRS provides expert regulatory and quality support to bring generic and well-established pharmaceuticals, medical devices, cosmetics and food supplements to the market. 

We are a team of pharmaceutical and medical device regulatory affairs and quality systems specialists with extensive experience from all different aspects of regulatory affairs and quality covering a wide range of products.

All consultants have long-term experience in the field, in leading and/or executing positions in international pharmaceutical and medical device industries and from regulatory authorities.

SRS is a growing company with 18 employees and a network of more than 20 specialized consultants/consultancies in various fields and countries.

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Management

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Ann-Cathrin Jareman
Managing Director

Ann-Cathrin has 25 years experience working with CE-marking, FDA-clearance, registration and quality systems for medical devices, including IVDs.

Mail: Anki@srs.se

Phone: +46 8 544 767 91

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Lars Jansson
Business Development,
Senior Expert

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

Mail: Lars@srs.se

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Charlotte Lewerth
Director Regulatory Affairs Pharmaceuticals

Charlotte has more than 15 years’ experience working within Regulatory Affairs in several pharmaceutical companies and since 2012 as head of Regulatory Affairs.
 

Mail: Charlotte@srs.se

Phone: +46 8 121 326 71

Marie Lindholm
Director Quality Pharmaceuticals
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Marie has more than 15 years experience in Quality Assurance working with manufacturing, supplier handling and audits in several Pharmaceutical companies, including QP and RP roles. 
 

Mail: Marie@srs.se

Phone: +46 8 121 326 74

Karin Rye
Director Medical Device
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Karin has more than 13 years experience in Regulatory Affairs from several medical device companies, working with product development, CE-marking, registrations outside EU, medical device vigilance and Quality Assurance.

Mail: Rye@srs.se

Phone: +46 8 121 326 75

Collaborations

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Through the international network, PharmaPriceinternational, PPI,

we have access to pricing and reimbursement experts in the major geographies in the world. In this network, SRS is responsible for the Nordic countries.

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Scandinavian Regulatory Services is a founding member of EuDRAcon, a pan-European network of regulatory affairs consultancy companies dealing with medicinal products, medical devices, cosmetics and food supplements. Through this network we always have easy and quick access to qualified regulatory input from all countries in Europe