Skip to content
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
February 2019

EURORDIS response to European Ombudsman strategic inquiry into pre-submission activities organised by the European Medicines Agency


The European Ombudsman has requested the opinion of interested parties on how the European Medicines Agency conducts pre-authorisation activities on medicines. This document is the EURORDIS response to that inquiry, setting out why the current system is robust and vital to ensure that clinical development is well designed and with input of patients.

(January 2019)

This site is registered on wpml.org as a development site.