Forms, Policies & Procedures

Here you will find a repository of forms, policies and procedures related to research at the University of Delaware. This repository draws on sources throughout campus to provide quick and easy access to these resources in a variety of formats, such as html, MSWord and Adobe PDF. We encourage you to explore and use the tools provided to narrow your search by word, resource type or category in order to learn more about the content that governs research at UD.
RO Forms, Policies, and Procedures Search 2019

Animal Subjects in Research

For Forms, Policies and Procedures pertaining to Animal Subjects in Research and other resources

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Conflict of Interest
Contracts and Grant Management
Effort Certification
Export Regulations (ITAR/EAR/OFAC)
Human Subjects in Research
Intellectual Property
Internal Funding
Material Transfer
Reporting Misconduct
Research Administration
Research Agreement Templates
RO Forms, Policies, and Procedures Search 2019
Forms, Policies and Procedures (2 Procedures Entries)
Procedure: Intellectual Property
NIH Manuscript Submission Portal

NIH Manuscript Submission Portal

  1. Deposit Files: Anyone can submit; however, an author or PI should serve as the reviewer. Reviewers are notified of submissions via e-mail.
  2. Initial Approval: Reviewer associates funding and approves the material for processing.
  3. NIHMS Conversion: NIHMS converts complete deposits to PMC-ready documents and notifies the reviewer via e-mail when they’re available. (approx. two to three weeks)
  4. Final Approval: Reviewer requests corrections to, or approves, PMC-ready documents for inclusion in PMC.
  5. PMCID Assigned: A PMCID is assigned when Final approval is complete and the manuscript is matched to a PubMed Record.

The NIH Manuscript Submission (NIHMS) system supports the deposit of manuscripts into PubMed Central (PMC), as required by the public access policies of NIH and other participating funders.


Procedure Details:

OWNER: National Institutes of Health


Procedure Source Email

Procedure: Intellectual Property
Preparing a Sequence Listing for the USPTO

Preparing a Sequence Listing for the USPTO

This procedure has been developed to assist in protecting the intellectual property generated by research. Please review the material carefully and if there are any questions, please refer to the Regulatory Affairs page.

These instructions are based on the U.S. Code of Federal Regulations, 37 CFR Sections 1.821-1.825. The sequence rules require the use of standard symbols and a standard format for sequence data and submission of the data in computer readable form. The sequence listing must be in ASCII text. Instructions for formatting the sequence listing and a sample sequence listing are presented on the following pages. The USPTO has a software program, “PatentIn,” to help you prepare sequence listings in the proper format.You can download the software and obtain instructions for using the software from


Procedure Details:

OWNER: Research Office


Procedure Source Email


Compliance Hotline
Phone: (302) 831-2792

UD Research Office
210 Hullihen Hall
Newark, DE 19716
Phone: (302) 831-2136
Fax: (302) 831-2828
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