Nordic consultants in regulatory affairs, quality assurance, pharmacovigilance and market access.

Nordic Regulatory Affairs expertise

We know the Nordic markets. Whether you are looking for regulatory support to manage a project, a product launch, or cover a role in your organisation – we have the flexibility to meet your needs. We offer compliance support and local regulatory intelligence across Sweden, Denmark, Finland, Norway and Iceland to give you a competitive advantage.

Nordic regulatory affairs experts

Our experienced specialists can take on full responsibility for all your Nordic regulatory affairs activities. This means managing the full regulatory lifecycle in the Nordic markets and handling all local requirements e.g. labelling and product information, authority communication and regulatory intelligence.  

Database management is provided by specialists with deep understanding of the local requirements, ensuring correct management of FASS, LiiV, Felleskatalogen, Pharmaca Fennica and DKMAnet.

We also offer experienced specialists to project manage production and review of common artworks for all the Nordic markets.

Nordic compliance services

Your contact person

Staffan Thunell

Founding partner

BSc Economics and BA

Staffan has a long background in entrepreneurship within the life science industry. He has 20+ years experience from posit­ions as Founder, Chair­man, CEO and CFO within medical affairs consulting and small pharma. Previously Staffan worked in executive positions in big pharma and specialty pharma companies.