Search
Our dedicated regulatory team has in-depth knowledge of the life sciences regulatory environment with team members having experience at the EU Commission, the Danish Medicines Agency, the Danish Veterinary and Food Administration and rights-granting bodies such as EUIPO. This enables us to provide pragmatic, actionable guidance to help clients navigate complex regulations and landscapes.
We support all innovative stakeholders in the life sciences ecosystem, providing legal and strategic guidance throughout the chain, from early R&D to post-market compliance. Our services include support for pre-clinical and clinical trials and investigations, product approvals, company authorisations and permits, market access, CE marking, manufacturing and distribution, pricing and reimbursement, promotional activities, affiliation and transparency, data and regulatory exclusivity, competition and procurement law, data privacy, industry compliance matters and requirements relating to ESG and sanctions.
We support all markets in the Nordic region, coordinating across and participating in European and international life sciences expert networks to offer a solid foundation for providing the highest level of expertise in the field.