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.
