DIRECT-TO-CONSUMER GENETIC TESTING: EMPOWERING EU CONSUMERS AND GIVING MEANING TO THE INFORMED CONSENT PROCESS WITHIN THE IVDR AND GDPR FRAMEWORKS. (In Vitro Diagnostic Regulation, European General Data Protection Regulation)
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DIRECT-TO-CONSUMER GENETIC TESTING: EMPOWERING EU CONSUMERS AND GIVING MEANING TO THE INFORMED CONSENT PROCESS WITHIN THE IVDR AND GDPR FRAMEWORKS. (In Vitro Diagnostic Regulation, European General Data Protection Regulation)
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This document cites
- Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
- Decision of the EEA Joint Committee No 13/2007 of 27 April 2007 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement
- Directive 95/46/EC of the European Parliament and of the Council of 24 October 1995 on the protection of individuals with regard to the processing of personal data and on the free movement of such data
- Directive (EU) 2015/1535 of the European Parliament and of the Council of 9 September 2015 laying down a procedure for the provision of information in the field of technical regulations and of rules on Information Society services (Text with EEA relevance)
- Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices
