Dialogue forum part 1

The Swedish Medical Products Agency's innovation office, in collaboration with SwedenBIO, invites you to webinars via Teams on four consecutive Tuesdays starting on May 24.

On May 24, the theme is Regulatory Processes Part 1 – Regulatory Framework for Drug Author ization. The aim is to provide an overview of the regulatory framework governing the authorization of medicines (Marketing Authorization).

The seminar will cover

  • Dialogue Forum (Medical Products Agency DG Björn Eriksson, Vice President SwedenBIO Frida Lawenius)
  • Mission and role of the authorities
  • The regulatory framework (horizontal)
  • Different types of new applications (legal basis).

The format is a 45-minute lecture followed by a 15-minute question and answer session. The webinars are open to all, but are mainly aimed at smaller pharmaceutical and medical device companies.

Read more and register here.