Informed consent form presentation upload
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This document discusses informed consent, which ensures patients and clinical trial participants are aware of potential risks and costs before treatment or procedures. Informed consent has two parts: an information sheet describing the nature of treatment, alternatives, risks and benefits; and a consent certificate. For consent to be valid, the participant must be competent and consent voluntarily without pressure, and they can withdraw consent if interests change. The consent process allows for free decision making through effective communication between all parties.
Informed consent form presentation upload
- 2. Introduction Informed consent is a legal procedure which ensures that: Patients ,Clients and Research paticipants are aware of all the potential risks and cost involved in a treatment or in medical procedures Example - clinical trial participant It consist of 2 parts Information sheet Consent Certificate
- 3. Criteria and Advantages Informing client on the nature of the treatment Possible alternative treatment The potiential risk and Benefit Participant must be competent and consent should be Voluntarily (to make form valid ) Free decision making Resigning of consent if interest is lost Document must not be signed immediately ( plenty of time ) Effective and transparent communication between clients, doctors &study directors