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.
*NOTE: As of October 2020 Google Chrome changed how it handles file downloads. If you encounter difficulties, right click on the “Download” button/link and select “save link as.” Once selected the file download will be executed and can be saved to the desktop. A second method is to use a different browser.
Animal Subjects in Research
For Forms, Policies and Procedures pertaining to Animal Subjects in Research and other resources
Compliance
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
Safety
Students
Templates
University
Procedure: NIH
NIH Manuscript Submission Portal
NIH Manuscript Submission Portal
- Deposit Files:
Anyone can submit; however, an author or PI should serve as the reviewer. Reviewers are notified of submissions via e-mail. - Initial Approval: Reviewer associates funding and approves the material for processing.
- 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) - Final Approval:
Reviewer requests corrections to, or approves, PMC-ready documents for inclusion in PMC. - 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
RESPONSIBLE OFFICE: Research Office
Procedure Source
Email
Procedure: Research Office
Preparing a Sequence Listing for the USPTO
Preparing a Sequence Listing for the USPTO
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 Patentin Software
Related Links
Procedure Details:
OWNER: Research Office
RESPONSIBLE OFFICE: Research Office
Procedure Source
Email