The aim of the two-day conference is to clarify country specific requirements for conducting clinical trials in the Nordic countries and strengthen cooperation between professionals. Current practical aspects of managing clinical trials in the region will be presented, both country by country and from a Nordic study management´s perspective. Aspects of creating a Nordic organization will be addressed and the possibility to use health registers in clinical research will be discussed.
Regulatory representatives from the different countries will present their GCP-inspection work and the Inspectors Working Group within EMA.
This conference will provide an opportunity to interact and converse with colleagues from the different Nordic countries!
The conference is organized in cooperation with the associations of the pharmaceutical industries in the Nordic countries.
It will be an opportunity to meet colleagues and listen to regulatory authority representatives and key actors in the field.
Course fee (SEK excl. VAT, early/late) : 5300/6400 SEK after 2010-08-31
For more information and the whole program
Register today!