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.
