Home
Forms Library
(IRB approval valid for 1 year) Expedited (explain) - Wheelock College - wheelock

(IRB approval valid for 1 year) Expedited (explain) - Wheelock College - wheelock 2025

(IRB approval valid for 1 year) Expedited (explain) - Wheelock College - wheelock Preview on Page 1

Show details

4.5 out of 5

54 votes

The document outlines the guidelines and procedures for the Institutional Review Board (IRB) at Wheelock College, detailing its purpose to protect the rights and welfare of human research participants. It includes information on federal compliance, responsibilities of researchers, review procedures for new and previously approved projects, informed consent requirements, and specific considerations for vulnerable populations such as children. The document also provides appendices with forms and examples related to IRB processes.

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.

The fastest way to redact (IRB approval valid for 1 year) Expedited (explain) - Wheelock College - wheelock online

Ease of Setup

DocHub User Ratings on G2

Ease of Use

DocHub User Ratings on G2

Dochub is the greatest editor for updating your forms online. Adhere to this simple guide to redact (IRB approval valid for 1 year) Expedited (explain) - Wheelock College - wheelock in PDF format online for free:

Register and log in. Create a free account, set a secure password, and proceed with email verification to start managing your forms.
Add a document. Click on New Document and choose the file importing option: add (IRB approval valid for 1 year) Expedited (explain) - Wheelock College - wheelock from your device, the cloud, or a protected URL.
Make changes to the sample. Take advantage of the top and left panel tools to modify (IRB approval valid for 1 year) Expedited (explain) - Wheelock College - wheelock. Add and customize text, images, and fillable areas, whiteout unneeded details, highlight the significant ones, and provide comments on your updates.
Get your documentation done. Send the sample to other parties via email, generate a link for quicker file sharing, export the sample 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.

What does it mean to be IRB approved for a study?

Expedited Review: Review of proposed research by the IRB Chair or a designated voting member or group of voting members, rather than by the entire IRB Committee. Federal rules permit expedited review for certain kinds of research involving no more than minimal risk and for minor changes in approved research.

What is expedited IRB approval?

Expedited review (Level II review), is a procedure through which certain kinds of research may be reviewed and approved without convening a meeting of the entire IRB.

What happens after IRB approval?

Meets regulatory definitions of both research and human subjects (a.k.a. regulated research). IRB review IS required. Research may not begin without approval.

How long is an IRB approval valid?

Under FDA regulations, an Institutional Review Board is group that has been formally designated to review and monitor biomedical research involving human subjects. In ance with FDA regulations, an IRB has the authority to approve, require modifications in (to secure approval), or disapprove research.

What does IRB approval mean?

After IRB approval, any subsequent changes to the study must be reviewed and approved by the IRB prior to implementation. This includes changes to the research team, recruitment process or material, consent procedures or materials, participant payment, data collection procedures, and target population.