Regulatory processes part 4 – Clinical trials of medical devices.
The aim is to provide an overview of regulatory frameworks governing clinical trials of medical devices. The seminar will cover
- Mission and role of the authorities
- The regulatory framework (horizontal)
- Tips and advice.
Speaker: Elin Karlberg, Head of the Regulatory Group in Clinical Trials, 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.
