Clinical Trials

Ethical Standards of The Study

Ethical Standards of The Study

Our site has SOP( standardized operating procedures) for obtaining Informed consent.Participants are communicated about the purposes of the research, its expected duration, and the nature of any interventions/experiments,anticipated risks and benefits of participation and the reasonable alternatives to participation in the research protocol,confidentiality provisions relating to the research records,any compensation and/or treatment available for research related injuries,the right to not participate and to discontinue participation at any time without penalty,Informed consent will be documented appropriately.

In the modern conception, consent to a therapy or a research protocol must possess three features in order to be valid. It should be voluntarily expressed, it should be the expression of a competent subject, and the subject should be adequately informed.

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