The US Department of Health and Human Services, Office of Human Research Protection: http://www.hhs.gov/ohrp/

The Common Rule and DHHS Regulations (45 CFR 46): http://ohsr.od.nih.gov/guidelines/45cfr46.html

The Belmont Report: http://www.fda.gov/oc/ohrt/IRBS/belmont.html

The US Department of Health and Human Services, Food and Drug Administration: http://www.fda.gov/

FDA Regulations:

• Electronic Record (21 CFR 11): http://www.access.gpo.gov/nara/cfr/waisidx_00/21cfr11_00.html

• Protection of Human Subjects (21 CFR 50): http://www.access.gpo.gov/nara/cfr/waisidx_00/21cfr50_00.html

• Institutional Review Boards (21 CFR 56): http://www.access.gpo.gov/nara/cfr/waisidx_00/21cfr56_00.html

Good Clinical Practice in FDA-Regulated Clinical Trials

Dana Farber/Harvard Cancer Center Protocol Forms (requires BIDMC authentication for redirection)

BIDMC Normal Lab Reference Range List