Regulatory processes part 2 – Strategic and practical aspects of drug approval.
The aim is to provide an overview of the regulatory aspects of bringing a medicine to the market. The seminar will cover
- How is an application structured
- Choice of authorization procedure – strategic challenges
- What help is available? Regulatory and scientific advice (national/central).
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.
