Dialogue forum part 3

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

Regulatory processes part 3 – Regulatory framework for human clinical trials.

The aim is to provide an overview of the regulatory framework governing clinical trials. The seminar will cover

  • Mission and role of the authorities
  • The regulatory framework (horizontal)
  • Tips and advice.

Speaker: Gunilla Andrew-Nielsen, Head of Unit for Clinical Trials and Licenses, Medical Products Agency.

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.