1. Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
2. Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 Apr 2017
3. Regulation (EU) 2017/746 of the European Parliament and of the Council 5 Apr 2017
4. Badnjević A, Pokvić LG, Džemić Z et al (2020) Risks of emergency use authorizations for medical products during outbreak situations: a COVID-19 case study. BioMed Eng OnLine 19:75
5. Badnjević A, Cifrek M, Magjarević R, Džemić Z (eds) Inspection of medical devices. In: Series in biomedical engineering. Springer, Singapore