Skip to Main Content
It looks like you're using Internet Explorer 11 or older. This website works best with modern browsers such as the latest versions of Chrome, Firefox, Safari, and Edge. If you continue with this browser, you may see unexpected results.

Interim Research Projects and Preprints: Home

Overview

The NIH is encouraging all researchers to take advantage of the public dissemination of preprints and other interim research projects. This guide will explain the process according to the NIH rules.

Preprint process to Postprint Life Cycle

Preprint postprint published By Thomas Shafee - Own work; adapted from diagram by Ginny Barbour, CC BY 4.0

NIH ANNOUNCEMENT

Notice Number NOT-OD-17-050 on March 24, 2017 announced the new NIH policy on preprints and interim research products, Reporting Preprints and Other Interim Research Products. Effective May 25, 2017, the information regarding preprint and IRP use and citations in NIH forms can be used.  This announcement is available on the NIH website.

What are Interim Research Products?

Interim Research Products (IRPs) are defined by the NIH as "...complete, public research products that are not final".

A preprint is often complete and public draft of a scientific document. These unreviewed manuscripts are written using a peer-reviewed journal article style. Preprints are often released to "speed dissemination, establish priority, obtain feedback, and offset publication bias". 

A preregistered protocol is another commen type of iterim product. A researcher wil publicly declare key elements of their research protocol in advance. The reasoning can be to "enhance the rigor of their work".

Notes:

  • You are not required to create interim research products through your NIH award.
  • Applicants are not required to cite interim research products as part of their grant applications.
  • Preprints do not fall under the NIH public access policy because they are not published in peer-reviewed journals.
  • This guide notice does not apply to clinical trial registration. For registration of clinical trial protocols information see ClinicalTrials.gov.

Why Provide IRPs

There are several purposes for making preprints or other interim research products publication available.

  • Establishing priority (release information and get a "timestamp" on your work).
  •  Peer review and the editorial process can be slow so this allows the work to be accessible and you can refer to it in other publications, a grant application or grant progress reports.