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The Atlanta Clinical & Translational Science Institute has kindly shared their Ethical Dilemmas in Scientific Research and Professional Integrity website, video, and podcast with each CTSA.
This web page presents 40+ case scenarios involving responsible conduct in research. Each case is followed by a brief, expert opinion that suggests strategies for resolution. These resources have proven useful as teaching aids and are broadly relevant across the research spectrum. Please help us spread the word!
The Library of the Health Sciences offers workshops focused on instruction and consultation in locating and evaluating scientific research indexed in scholarly databases (e.g., Medline, Embase) and in grey (unpublished) literature.
PubMed Central® (PMC) is a free archive of biomedical and life sciences journal literature at the U.S. National Institutes of Health's National Library of Medicine (NIH/NLM). In keeping with NLM’s legislative mandate to collect and preserve the biomedical literature, PMC serves as a digital counterpart to NLM’s extensive print journal collection.
This program is designed for highly motivated undergraduate and graduate students who are interested in exploring potential careers in the health sciences, and is focused on familiarizing them with biomedical research and practice opportunities.
The Chicago Community Research Map is a resource to find out about the health-related research taking place in the community. This information is available to research investigators, community organizations and any individual interested to know more about the research taking place in Chicago and its communities.
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
Clinical Research Boot Camp is an intensive 3-day training program tailored to meet the specific needs of clinical research personnel and teach them to carry out successful clinical research studies.
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).