Get consent to share information template

(in-FORMD kun-SENT) A process in which patients are given important information, including possible risks and benefits, about a medical procedure or treatment, genetic testing, or a clinical trial. This is to help them decide if they want to be treated, tested, or take part in the trial.

the patient giving consent must have capacity • the consent must be freely given • the consent must be sufficiently specific to the procedure or treatment proposed • the consent must be informed. The four criteria for a valid consent must be met irrespective of whether the consent is in writing or oral.

The main purpose of the informed consent process is to protect the patient. A consent form is a legal document that ensures an ongoing communication process between you and your health care provider.

Informed consent is a person's decision, given voluntarily, to agree to a healthcare treatment, procedure or other intervention that is made: Following the provision of accurate and relevant information about the healthcare intervention and alternative options available; and.

Informed consent means that you make your decision after your health care provider has explained the benefits and risks of the recommended test, treatment or procedure, and any options that are available to you.

Informed consent of a person must be sought before any treatment, medical or otherwise, is provided, administered, or given. Consent is not only agreeing to a treatment or intervention, it should be given in an informed way, with consideration given to all available options.

Valid informed consent for research must include three major elements: (1) disclosure of information, (2) competency of the patient (or surrogate) to make a decision, and (3) voluntary nature of the decision.