1. Council Directive 93/42/EEC of 14 June 1993 concerning medical devices, OJ. (1993). L 169(36), 1–43.
2. European Parliament CotEU. (1990). Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices. Official Journal L.,189(20/07), 0017–0036.
3. Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices, OJ. (1998). L 331(41), 1–37.
4. Carr, A. (2017). Follow-up of patients with metal-on-metal hip replacements. BMJ,2017(358), 2017. https://doi.org/10.1136/bmj.j3387. (Published 18 July).
5. Heneghan, C., Aronson, J. K., Goldacre, B., Mahtani, K. R., Plüddemann, A., & Onakpoya, I. (2017). Transvaginal mesh failure: Lessons for regulation of implantable devices. BMJ,7(359), j5515. https://doi.org/10.1136/bmj.j5515.