1. Summary of the HIPAA privacy rule. Available at: http://www.hhs.gov/hipaa/for-professionals/privacy/laws-regulations/index.html. [accessed 15.03.16].
2. Guidance for industry and FDA staff, In Vitro Diagnostic (IVD) device studies – frequently asked questions. Available at: http://www.fda.gov/downloads/MedicalDevices/.../ucm071230.pdf. [accessed 15.03.16].
3. The Belmont report. Available at: http://www.hhs.gov/ohrp/humansubjects/guidance/belmont.html. [accessed 15.03.16].
4. Informed consent for in vitro diagnostic device studies using leftover human specimens that are not individually identifiable. Available at: http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm078384.htm. [accessed 15.03.16].
5. How can covered entities use and disclose protected health information for research and comply with the privacy rule? Available at: https://privacyruleandresearch.nih.gov/pr_08.asp. [accessed 15.03.16].