1. 2013
2. Guideline
3. The Approximation of the Laws, Regulations and Administrative Provisions of the Member States Relating to the Implementation of Good Clinical Practice in the Conduct of Clinical Trials on Medicinal Products for Human Use.
4. European Medicines AgencyRevised Framework for Interaction Between the European Medicines Agency and Patients and Consumers and Their Organisations2014
5. Patient Involvement in Pharmaceutical Industry-Led Medicines R&D2016