Evidence-based maintenance of medical devices: Current shortage and pathway towards solution

Author:

Badnjevic Almir12

Affiliation:

1. Verlab Research Institute, Sarajevo, Bosnia and Herzegovina

2. Faculty of Pharmacy, University of Sarajevo, Bosnia and Herzegovina

Publisher

IOS Press

Subject

Health Informatics,Biomedical Engineering,Information Systems,Biomaterials,Bioengineering,Biophysics

Reference29 articles.

1. Senbekov M et al. The recent progress and applications of digital technologies in healthcare: a review. International journal of telemedicine and applications 2020 (2020).

2. Health Canada Guidance Document: Guidance for the Labelling of Medical Devices, not including in vitro diagnostic devices – Appendices for the Labelling of Soft, Decorative, Contact Lenses and Menstrual Tampons. Health Canada Guidance Document, (June 18, 2015).

3. EU Medical Device Regulation: Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC. Official Journal of the European Union, L 117, (May 05, 2017).

4. EU Medical Device Regulation: Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety. Official Journal of the European Communities, L 31, (February 01, 2002).

5. Post-market Surveillance of Medical Devices: A Revie;Badnjević;Technology and Health Care.,2022

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