OHRP (Office for Human Research Protections)http://www.hhs.gov/ohrp/outreach/
CenterWatchhttp://www.centerwatch.com/
Clinical Trials.govhttp://www.clinicaltrials.gov/
National Cancer Institutehttp://www.cancer.gov/
National Institute of Healthhttp://www.nih.gov/
FDA (Food & Drug Administration)http://www.fda.gov/
- Center for Drug Evaluation and Research (CDER)
- CDER Home
- Regulatory Guidance
- IND - Guidance on the preparation of an investigator-held Investigational New Drug (IND) Application.
- Center for Devices and Radiological Health (CDRH)
- CDRH Home
- Device Advice
- IDE - Guidance on the preparation of an investigational device exemption (IDE).
- Center for Biologics Evaluation and Research (CBER)
- Clinical Trials & GCP
- Guidance for Instiutional Review Boards and Clinical Investigators - Compilation of current FDA Guidance documents for IRBs, including investigator responsibilities. Includes information on both drug and device studies.
FDA for Kidshttp://www.fda.gov/oc/opacom/kids/default.htm
FDA's MedWatchhttp://www.fda.gov/medwatch/
President's Council on Bioethicshttp://bioethics.gov/
Ethical, Legal, and Social Implications (ELSI) of Human Genetics Researchhttp://www.genome.gov/ELSI/
Public Responsibility in Medicine and Research/The Applied Research Ethics National Association (PRIM&R/ARENA)http://www.primr.org/
Kids for Researchhttp://www.kids4research.org/
Kids Healthhttp://kidshealth.org/kid/word/
Human Genomehttp://www.genome.gov/Pages/EducationKit/
Medline Plushttp://medlineplus.gov/
Tri-Institutional Human Embryonic Stem Cell Researchhttp://trisci.org/
Clinical and Translational Science Center (WCMC)http://www.med.cornell.edu/CTSC/
