REQUIREMENTS FOR CONSENT TO CONDUCT RESEARCH, TREATMENT OR DIAGNOSTICS IN THE AREA OF HUMAN GENOME
- Authors: Povarov Y.S.1
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Affiliations:
- Department of Civil and Business Law, Samara National Research University
- Issue: Vol 5, No 2 (2019)
- Pages: 23-28
- Section: Civil law
- URL: https://journals.ssau.ru/jjsu/article/view/7112
- DOI: https://doi.org/10.18287/2542-047X-2019-5-2-23-28
- ID: 7112
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Full Text
Abstract
The article is about the attribute characteristics of consent to conduct research (treatment, diagnosis) in the field of the human genome, enshrined in international and domestic legal acts, while revealing the autonomy and interrelation of relevant features. Considering that the collection of genetic information can be carried out in order to provide medical care and be accompanied by medical intervention, increased attention is paid to legal indications of consent to such an intervention (information of the person concerned, voluntariness and preliminary nature of consent, its clear expression). The author, among other things, emphasizes the need for legislative regulation (in the format of a multi-factor approach) of the temporal aspect of conciliation procedure; indicates the relevance of applying the rule of giving medical clarifications in the situation of a request for termination of medical intervention; justifies the expediency of considering the sign of an obvious expression of consent, first of all, from the position of the form of expression of consent and in the content-organizational plan.
About the authors
Yu. S. Povarov
Department of Civil and Business Law, Samara National Research University
Author for correspondence.
Email: grigorjewa.katerina@yandex.ru
Russian Federation
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