Let us know in advance which area(s) you have questions about. For example, we answer questions about
- Clinical trial protocol
- Manufacturing of medicines under development
- Preclinical development
- Choice of procedure to obtain a marketing authorization in Sweden or in the EU.
There are a limited number of places and a maximum of two are accepted per company. It is first come, first served. You will receive feedback once the registration period has expired, informing you whether you have a place and when you are welcome. Send your registration by November 11.
Read more and register here.