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The NIH Public Access Policy requires investigators to deposit an electronic version of articles resulting from NIH funding to PubMed Central (PMC) upon acceptance for publication
Bioethics Resources on the Web provides a compilation of web links to information of potential use and interest to diverse audiences—biomedical and behavioral researchers, health care professionals, research participants, patients and patient advocates, students and faculty in different disciplines, and the general public.
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).
If you are experiencing computational, data storage or networking bottlenecks on traditional user/lab workstations and/or you are considering using cloud for your research, SABER can be an effective solution both in terms of function and cost.
SABER will operate on a pay-per-use basis, providing researchers with the flexibility to pay for used time/storage and ensures a good return on investment. Researchers can learn more about SABER specs, their competitive rate structure and order process here.
The Centers for Disease Control and Prevention provide information on human participant protection in clinical investigations involving human subjects and the use of drugs, biologics or devices.
The Smart Chicago Collaborative and the Chicago Department of Public Health believe data should be accurate, transparent and easy to understand. We created the Chicago Health Atlas so that you can review, explore and compare health-related data over time and across communities. In addition, the Chicago Health Atlas provides a place for residents to see our progress implementing Healthy Chicago 2.0, the citywide plan to improve health equity.
Our hope is that you will use this data to both better understand health in Chicago and identify opportunities to improve health and well-being.
The Chicago Health Atlas is, by design, an
FDA regulations and guidance documents are accessible from this site as well as international GCP guidance documents on which FDA has collaborated and that have been adopted as official FDA guidance.
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."