Home
Forms Library
Example of an Informed Consent Document - University at Buffalo

Get the up-to-date Example of an Informed Consent Document - University at Buffalo 2025 now

Example of an Informed Consent Document - University at Buffalo Preview on Page 1

Show details

4.4 out of 5

41 votes

The document is an example of an Informed Consent Document for a research study conducted by the Children & Youth Institutional Review Board (CYIRB) at the University at Buffalo. It outlines the ethical principles of informed consent, detailing participants' rights, study purpose, procedures, risks, benefits, confidentiality, and compensation. The document emphasizes voluntary participation and provides guidelines for parental permission for minors. It also includes sections on health information disclosure and participant withdrawal rights.

Here's how it works

01. Edit your form online

Type text, add images, blackout confidential details, add comments, highlights and more.

02. Sign it in a few clicks

Draw your signature, type it, upload its image, or use your mobile device as a signature pad.

03. Share your form with others

Send it via email, link, or fax. You can also download it, export it or print it out.

How to quickly redact Example of an Informed Consent Document - University at Buffalo online

Ease of Setup

DocHub User Ratings on G2

Ease of Use

DocHub User Ratings on G2

Dochub is a perfect editor for updating your forms online. Follow this straightforward guide to redact Example of an Informed Consent Document - University at Buffalo in PDF format online at no cost:

Register and sign in. Register for a free account, set a secure password, and go through email verification to start managing your forms.
Add a document. Click on New Document and select the form importing option: upload Example of an Informed Consent Document - University at Buffalo from your device, the cloud, or a protected link.
Make adjustments to the template. Take advantage of the top and left-side panel tools to change Example of an Informed Consent Document - University at Buffalo. Insert and customize text, images, and fillable areas, whiteout unneeded details, highlight the important ones, and comment on your updates.
Get your documentation completed. Send the form to other people via email, create a link for faster file sharing, export the template to the cloud, or save it on your device in the current version or with Audit Trail added.

Try all the benefits of our editor today!

be ready to get more

Complete this form in 5 minutes or less

Get form

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.

How to write an informed consent document?

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.

What information must be included on an informed consent document?

Function The nature of the procedure or intervention. The risks and benefits of the procedure or intervention. Reasonable alternatives. The risks and benefits of alternatives. An assessment of the patients understanding of these elements [10][11]

Which of the following must be included in an informed consent document?

Elements of an Informed Consent Form Expected duration of the subjects participation. Explanation of the procedures to be followed. Attendant risks or discomforts. Expected benefits (money, course credit, free physical examination).

What are the 4 components of informed consent?

Basic Elements of Informed Consent Purpose of the Research. Description of the Research. Risks. Benefits. Alternatives to Participation.

What is an example of informed consent statement?

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.

Related forms

be ready to get more

Complete this form in 5 minutes or less

Get form

What information must be included in informed consent?

Obtaining informed consent in medicine is a process that should include describing the proposed intervention, emphasizing the patients role in decision-making, discussing alternatives to the proposed intervention, discussing the risks and benefits of the proposed intervention, and eliciting the patients preference,

Get the up-to-date Example of an Informed Consent Document - University at Buffalo 2025 now

Here's how it works

How to quickly redact Example of an Informed Consent Document - University at Buffalo online

Complete this form in 5 minutes or less

Got questions?

How to write an informed consent document?

What information must be included on an informed consent document?

Which of the following must be included in an informed consent document?

What are the 4 components of informed consent?

What is an example of informed consent statement?

Complete this form in 5 minutes or less

People also ask

What information must be included in informed consent?

Related links

Try more PDF tools