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The Office for the Protection of Research Subjects (OPRS) provides administrative support for the review and approval of research protocols (experiments) involving humans and human embryonic stem cells (hES).
The CCTS collaborated with members of the Office of the OVCR Quality Improvement Program to develop a set of standard case report forms. The forms should be useful for any investigator initiated clinical trials and can be customized to an individual study.
Investigators who need to translate a research protocol into lay language for informed consent documents and/or IRB submission may benefit from the University of Michigan’s "Simplification Guide to Medical Terms."
The HTS facility offers users the ability to screen biological targets against a library of over 100,000 unique chemical compounds in a time-efficient manner. HTS offers assistance with many of the early drug-discovery stages, including assay development and optimization, robotic screening, data analysis and interpretation, and hit validation.
ClinicalTrials.gov is a registry and results database of publicly and privately supported clinical studies of human participants conducted around the world. Investigators can learn more about national clinical studies, including relevant history, policies, and laws.
The CCTS's Biomedical Informatics Core manages the Clinical Research Data Warehouse. Campus investigators can work with Biomedical Informatics specialists to gain access to the warehouse and obtain both data counts and data extracts.
VIReC develops resources for and provides guidance to VA researchers using VA data. Their mission is to improve the quality of VA research that utilizes databases and information systems.