Medical device directive & Clinical investigation : Impact of the new regulation on clinical nvestiagation in Belgium, Steve Eglem, FAMHP
September 9, 2018
The BAREC Steering Board is pleased to invite you on a Symposium that will take place on Saturday 24 November 2018, from 9:00 till 12:30.
9:00 : Welcome
9:30 : Challenges for the ethics committees in Belgium anno 2018: state of the art. [BAREC Steering Board]
10:10 : Impact of the GDPR and the new biobank legislation on ethical review of clinical research. [Audrey Van Scharen, UZ Brussel]
10:50 : Break
11:20 : Compensation of subjects for their participation in clinical trials. [Josse Thomas, UZ Leuven]
End anticipated at 12:30.
Location: Auditoire central Maisin, UCL Woluwé.
Sandwiches and beverages will be provided.
Accreditation for economics and ethics has been applied for.
May 22, 2017
Moniteur Belge - Belgisch Staatsblad N.39 22 May 2017 : Loi relative aux essais cliniques de médicaments à usage humain - Wet betreffende klinische proeven met geneesmiddelen voor menselijk gebruik
Clinical trial on medicinal products : draft law introduced in the house on February 17, 2017
E-mail : webmaster[@]barec.be
Date de création : 01/06/2017