Clinical Research

Informed Consent Procedure in Clinical Trials

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Informed Consent in clinical trial is often the most important part of clinical trial and sometimes neglected too, resulting in serious consequences, for the patient, the doctor involved in the trial and the pharmaceutical company sponsoring the trial. Which brings us to the question of what exactly is an Informed Consent Procedure? It is process […]

Clinical Research

Informed Consent Process in Clinical Trials

Posted on

Informed Consent Procedure Before a clinical trial the researcher and participant engage in an agreement called an informed consent. The informed consent is firstly a written document outlining the procedure and possible effects and risks to the participant. It also describes the liability of the researcher and that of the volunteer. Any aftercare is also […]