Belgian Regulatory Affairs Society
BRAS is a professional organisation of people involved in regulatory affairs that supports its members to achieve the highest standards through information and training, and participates on an active and constructive way to the policymaking within the pharmaceutical and related sectors.
In almost all countries of the world, governments evaluate the safety, quality & efficacy aspects of products which may present a risk to their citizens. Regulations relating to standards and products are multiple, varied and developing.
Pharmaceutical and other directives are so complex that it was necessary to develop a new scientific discipline that has become known as "Regulatory Affairs".
BRAS Administrative Office will be on holidays as from 21 July 2017 until 15 August 2017 included. Have a nice summer !
Future courses & events
|21/09/17||Workshop on Market access in a hospital environment – future challenges|
|24/10/17||BRAS Symposium 2017|
|16/11/17||BRAS Advanced Course CTD module 3 – Quality section|
|28/11/17||Session on Medical Devices|
|14/12/17||Session on clinical trials - NEW DATE|