- Resources for Clinical Research
- Resources for Basic Research
- Consultations and Requesting Services
- Funding Opportunities
- Billing and Financial Information
- Tools and Software
- Forms and Templates
- Scientific Review
Need help?
Contact our Research Navigator for help locating resources, initiating a new study, or finding your way through the research process.
Contact Melissa Hansen, MLS, directly at 612-626-2318 or ctsi@umn.edu.
Clinical Translational Research (CTR) Portal
CTSI's Clinical Translational Research (CTR) Portal is an interactive, web-based system designed to provide targeted and secure access to research project information. The CTR Portal provides access to:
- request CTSI services;
- view and approve invoices for CTSI services;
- a list of your projects included in the CTSI database;
- links to helpful tools and systems;
- and news and information about CTSI.
Learn more about the CTR Portal, download forms and user guides, and view Frequently Asked Questions
REDCap
REDCap (Research Electronic Data Capture) is a secure web application designed exclusively to support data capture for research.
ResearchMatch
ResearchMatch is a recruitment tool that helps connect researchers and willing volunteers through a free, secure, web-based registry. ResearchMatch can be used for feasibility assessments or for recruitment.
Learn more about ResearchMatch at the University of Minnesota
Visit the ResearchMatch website
UMN Profiles
UMN Profiles is a research networking and expertise database. It not only shows publications, scientific expertise, and traditional directory information, but also illustrates how people are connected to others in the broad research community.
Learn more about UMN Profiles, watch a video, and view Frequently Asked Questions
MedDRA Web-Based Browser
To assist with the standardized reporting and aggregation of adverse events, CTSI now offers access to a subscription to MedDRA, the Medical Dictionary for Regulatory Activities. MedDRA is used to report adverse event data from clinical trials, and for post-marketing reports and pharmacovigilance. MedDRA is a pragmatic, clinically validated terminology that applies to all phases of drug development, excluding animal toxicology. It also applies to the health effects and malfunction of medical devices, and was developed by the International Conference on Harmonization (ICH).
To access MedDRA, log in to the web-based browser. Please log in using your username: 17195 and the MedDRA Web-Based Browser password: NXv6Hd41.