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Certain documents, including wills, codicils, testamentary trusts, divorce and adoption papers, some court orders, and notarized contracts, cannot typically be signed electronically.

The consent form must identify the subject's alternatives to participation in the protocol and should offer a discussion of their relative advantages and disadvantages. It is usually not necessary to provide a full account of the risks and benefits of alternative treatments in the research consent form.

' If properly obtained, an electronic signature can be considered an 'original' for the purposes of recordkeeping.” (would satisfy requirements of an audit). An electronic signature can include a “digital” signature on a consent document (such as using ) or a “I agree to participate” button in an online survey.

To create a consent form, you need to list the consenting parties and specify the activities or data covered by the consent. It should also state the parties' rights and responsibilities and include dates, contact information, and other necessary details.

4-Step Guide: How to Make a Consent Form Choose a sample consent form to customize. To begin, choose from a selection of sample consent forms and customize them easily to suit your specific needs. Adjust the form's design. Publish your form online. Get consent and print the documents if needed.

Electronic consent (e-consent) is a method of obtaining informed consent through the use of an electronic system instead of a paper consent form, e.g. in REDCap or .

Electronic signatures are not permitted to be used in executing wills or codicils, contracts relating to the alienation of immovable property, bills of exchange such as cheques, and long-term agreements for immovable property, which are in excess of ten years.

The revised Common Rule also states that ?informed consent shall be documented by the use of a written informed consent form approved by the IRB and signed (including in an electronic format) by the subject (participant)??.

Additionally, the consent document must be signed and dated by the patient (or the patient's legal guardian or representative). Many consent forms also require the healthcare practitioner's signature. Consent forms should include statements to be signed by the patient and the healthcare practitioner.