The law regulating clinical medical research aims to lay the foundations, standards, and controls necessary for conducting clinical medical research, and to protect the respondents, whether such research is preventive or diagnostic, curative or non-curative, interventional or non-invasive.
These researches are required to comply with the provisions of relevant laws, charters and regulations, provided that they are consistent with recognized international ethical standards and principles, all as indicated by the executive regulations of this law.
Below, we review the special procedures in the event of medical research being conducted on persons entitled to additional protection, in order to further guarantee their rights.
According to law
Medical research may not be restricted to a certain group of people or to groups entitled to additional protection unless the research is necessary and related to diseases specific to them, and with the availability of scientific and ethical justifications for their use, provided that the informed consent of each of them is obtained and if the medical research is Any of the categories entitled to additional protection must obtain the consent of the parents, or of those who have guardianship or guardianship in the event of the death of one or both parents, or from the legal representative, all in accordance with the controls and procedures specified by the executive regulations of this law.