About SRS
Experts within Regulatory Affairs and Quality Assurance since 1992
Karin Rye
Deputy Managing Director, Director Medical Device, Nutrition and Cosmetics
karin@srs.se +46 766 697 711Azadeh Foumani
Director Quality Assurance and Pharmacovigilance Pharmaceutical
azi@srs.se + 46 705 29 79 71
Charlotte Lewerth
Principal Expert Regulatory Affairs Pharmaceuticals
charlotte@srs.se +46 727 005 551
About SRS
At SRS we believe in the importance of maintaining a continuous supply of safe and effective medicines and medical devices. Through our business, we want to help companies provide safe and effective products to patients.
Our employees are experts in their respective fields with unique skills and perspectives. Our experienced team offers tailored solutions targeted to meet the specific needs of our customers.
In an industry that largely revolves around regulations, structures and processes we understand a company’s need for flexibility within the boundaries of the regulations. With over 30 years in the industry, we are an established partner to our clients.
With committment, customer focus and genuine knowledge, we contribute to the success of our customers.
History
Scandinavian Regulatory Services (SRS) was founded by Lars Janson over 30 years ago as one of the pioneering consultancy firms in pharmaceutical Quality Assurance and Regulatory Affairs, Lars’s decision to start the company stemmed from his experience in the pharmaceutical industry, including work at the Swedish MPA.
SBL and AGA were among SRS’s first clients. SBL was transitioning into a pharmaceutical company, while AGA, like all medicinal gas manufacturers, needed formal marketing authorizations for their products. With a limited number of available consultants, there was an abundance of work to be done. However, with support from Lars’s established international network, SRS successfully assisted these clients in achieving their objectives. This marked a strong beginning for the company, and since then, SRS has played a pivotal role in helping numerous companies enter the market. They’ve engaged in extensive discussions with the Swedish MPA, secured marketing authorizations for hundreds of products, formulated regulatory strategies for various types of products, and obtained over 60 wholesale distribution authorizations (GDP licenses).
After 20 years, the original company underwent a division, with Anki Jareman assuming the role of Managing Director. Anki brought her expertise in Regulatory Affairs/Quality Assurance (RA/QA) and medical device development to the company. SRS expanded its team to support both pharmaceuticals and medical devices and, over time, added food and cosmetics to its range of services.
The company’s success wouldn’t have been possible without the dedication and competence of everyone who has collaborated with SRS over the years, along with active participation in the established networks. Over the years, SRS has served more than 800 clients, many of whom have become repeat customers, hailing from nearly every corner of the globe.
Today, SRS continues its mission of assisting companies worldwide, with a particular emphasis on the European market, in bringing their products to market and maintaining a strong market presence.
