Create your Consent Agreement Form from scratch

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Here's how it works

01. Start with a blank Consent Agreement Form
Open the blank document in the editor, set the document view, and add extra pages if applicable.
02. Add and configure fillable fields
Use the top toolbar to insert fields like text and signature boxes, radio buttons, checkboxes, and more. Assign users to fields.
03. Distribute your form
Share your Consent Agreement Form in seconds via email or a link. You can also download it, export it, or print it out.

Craft Consent Agreement Form from the ground up by following these step-by-step guidelines

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Step 1: Open DocHub and get going.

Start by setting up a free DocHub account using any available sign-up method. Simply log in if you already have one.

Step 2: Sign up for a free 30-day trial.

Try out the whole collection of DocHub's pro features by signing up for a free 30-day trial of the Pro plan and proceed to build your Consent Agreement Form.

Step 3: Add a new blank form.

In your dashboard, hit the New Document button > scroll down and hit Create Blank Document. You’ll be taken to the editor.

Step 4: Organize the document’s view.

Utilize the Page Controls icon marked by the arrow to switch between two page views and layouts for more flexibility.

Step 5: Begin by adding fields to design the dynamic Consent Agreement Form.

Navigate through the top toolbar to place document fields. Insert and arrange text boxes, the signature block (if applicable), add photos, and other elements.

Step 6: Prepare and configure the added fields.

Configure the fillable areas you added based on your desired layout. Modify the size, font, and alignment to ensure the form is easy to use and polished.

Step 7: Finalize and share your form.

Save the ready-to-go copy in DocHub or in platforms like Google Drive or Dropbox, or design a new Consent Agreement Form. Send out your form via email or utilize a public link to engage with more people.

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Got questions?

We have answers to the most popular questions from our customers. If you can't find an answer to your question, please contact us.
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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.
If you prefer to write your own consent document, you may do so, but be sure to include all required elements of informed consent.
How to write a contract agreement in 7 steps. Determine the type of contract required. Confirm the necessary parties. Choose someone to draft the contract. Write the contract with the proper formatting. Review the written contract with a lawyer. Send the contract agreement for review or revisions.
Instructions for Developing an Informed Consent Document General Information. Describe the purpose(s) of this research study in lay terms. Purpose of the Study. Procedures. Risks. Benefits. Compensation, Costs and Reimbursement. Withdrawal or Termination from Study. Confidentiality.
To be legal and valid, informed consent must have three elements: It must contain all necessary information. A person signing the consent must have the mental capacity to comprehend the given information. It must be voluntary.
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Related Q&A to Consent Agreement Form

5 core concepts of consent 1 - Free and voluntary. Consent must be free and voluntary. 2 - Specific and informed. Consent must be specific and informed. 3 - Affirmative and communicated. 4 - Ongoing and mutual. 5 - Reflects capacity.
Simply put, yes, you can write your own legal contract. You just need to be sure to include key components such as an offer, an acceptance, an exchange of value, and the willingness of both parties to enter into a contract. Legally binding contracts can be done both in writing or orally.
How to write an agreement letter Title your document. Provide your personal information and the date. Include the recipients information. Address the recipient and write your introductory paragraph. Write a detailed body. Conclude your letter with a paragraph, closing remarks, and a signature. Sign your letter.
The informed consent process involves three key features: (1) disclosing to potential research subjects information needed to make an informed decision; (2) facilitating the understanding of what has been disclosed; and (3) promoting the voluntariness of the decision about whether or not to participate in the research.
The revised Common Rule requires the posting of IRB approved consent forms to a designated public federal website. The recipients of NIH funding must submit consent forms in ance with Section 46.116(h) of the revised regulations to ClinicalTrials.gov or to Regulations.gov (Docket ID: HHS-OPHS-2018-0021).

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