Informed Consent Form - Cardiology - HealthinCode 2025

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  1. Click ‘Get Form’ to open it in the editor.
  2. Begin by entering the patient’s full name in the designated field. This is crucial for identifying the individual consenting to the genetic study.
  3. Select the type of genetic study requested from the options provided. Ensure you check all relevant panels that apply to your case.
  4. In the Patient’s Authorization section, read through each statement carefully. Indicate your consent by selecting 'Yes' or 'No' where applicable.
  5. Complete the signature section by entering the name and National Identification Number of the patient or legal representative, followed by their signature and date.
  6. Finally, ensure that a physician signs off on the Statement of Existence of Informed Consent, confirming that all necessary information has been communicated.

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The primary types of informed consent weve covered include written, verbal, electronic, and implied consent. Each type serves specific research contexts and participant needs. Understanding Informed Consent is crucial for researchers to ensure participants are fully aware of the studys purpose, risks, and benefits.
Valid informed consent for research must include 3 major elements as follows: Disclosure of information. Competency of the patient (or surrogate) to make a decision. The voluntary nature of the decision.
To be valid, consent must be voluntary, informed, specific, current, and given by a person with capacity. Unless otherwise indicated, consent can be express or implied, written or verbal. Bundled authorisations may not meet the criteria for valid consent.