1. Medical devices: responsibility of the agent after the European regulations 2017/745 and 2017/746;Bouquet;Médecine Droit,2019
2. Ministry of health. Directorate of Medicines and Pharmacy. Circular N(7 of 19-02-1997 Consultative Commission for the Registration of Medical Devices. [internet]. Available from: http://dmp.sante.gov.ma/textes-legislatifs-et-reglementaires?rlc=853898.
3. Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices;French National Agency for Medicines,1990
4. Directive 93/42 CEE du 14 juin 1993 relative aux dispositifs médicaux (article 10 “Informations sur les incidents intervenus après la mise sur le marché”) [internet].;French National Agency for Medicines,1993
5. The Good Pharmacovigilance Practices Manual [internet];Ministry of Health,2020