1. U.S. Food and Drug Administration. (2023, July 17). Qualification of Medical Device Development Tools: Guidance for Industry, Tool Developers, and Food and Drug Administration Staff. Retrieved January 31, 2024, from https://www.fda.gov/regulatory-information/search-fda-guidance-documents/qualification-medical-device-development-tools.
2. The European Union Medical Device Regulation (2021, April 15). Commission Implementing Decision (EU) 2021/611. Retrieved January 31, 2024, from https://eur-lex.europa.eu/eli/dec_impl/2021/611.
3. Health Canada (2023, November 24). Medical Devices Regulations (SOR/98–282). Retrieved January 31, 2024, from https://laws-lois.justice.gc.ca/eng/regulations/sor-98-282/.
4. Jones, D. G. (1998). Anatomy and ethics: An exploration of some ethical dimensions of contemporary anatomy. Clinical Anatomy, 11(2), 100–105. https://doi.org/10.1002/(SICI)1098-2353(1998)11:2%3C100::AID-CA6%3E3.0.CO;2-Y.
5. Brekelmans, W. A. M., Poort, H. W., & Slooff, T. J. J. H. (1972). A new method to analyse the mechanical behaviour of skeletal parts. Acta Orthopaedica Scandinavica, 43(5), 301–317. https://doi.org/10.3109/17453677208998949.