Nordic-Baltic Regulatory Forum

What collaboration exists between the Nordic-Baltic countries and authorities today and what are the needs for tomorrow?

Get the authority perspective on the do’s and don’ts for Scientific advice – who to talk to, when and why.

Take part of the experiences and pro’s and con’s of Parallel Scientific Advice, RA-HTA-Industry.

Scout future trends within regulatory, get insight in Pharma Legislation EU revision and share reflections on how to prepare for the changing Regulatory roll, meeting the demands of being a Strategic partner and Project Lead.

Meet representatives from the Authorities and Industry and expand Your Regulatory network within the Nordic-Baltic region. Invest this half day in Your professional development!

Warmly Welcome to Your Regulatory Forum for Drug Development!

Who should attend?

Professionals with an interest in Regulatory affairs and Drug Development in the Nordic-Baltic area. We welcome participants from pharmaceutical companies, pharmaceutical industry associations, national competent authorities, contract research organizations, consultants and academia.

Program og påmelding

Program og påmelding på lakemedelsakademin.se