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Information for Prospective Participants in Research
Brochure “
Should I Participate in Research? Things I Need to Know” (for social science
and behavioral research)
en español
Becoming a
Research Volunteer: It’s Your Decision” by OHRP
Click
here
for NIH web site for senior health care issues, "Participating in Clinical
Trials"
To discuss concerns, obtain information, offer
input, click here
Information for Researchers
Graduate
Brochure (for graduate students and advisors)
After Approval
Brochure
Additional Resources
ETSU Home Page
ETSU Human Subject Training Program - CITI
Glossary
Special Interest Links
Request In-Service
Reference Library
Accreditation Standards
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National Committee on Quality Assurance (NCQA) Standards 2.1
Association on Accreditation of Human Research Protection Programs (AAHRPP) Standards
Clinical Trials Information
(Back to top)
Good Clinical Practice in FDA-Regulated Clinical Trials
Introduction to Clinical Trials (NIH)
Information for Sponsor-Investigators Submitting Investigational New Drug Applications (INDs)
FDA Clinical Trials Information for Consumers
FDA Clinical Trials Guidance for Researchers
Clinical Trials
Centerwatch Clinical Trials Listing Service
Ethical Conduct of Research
(Back to top)
The Belmont Report
Informe Belmont
Declaration of Helsinki
Declaracion de Helsinki
de la Asociacion Medica Mundial
Geneva Physicians Oath
ICH Code
Nuremberg Code
FWA Assurance Approvals
(Back to top)
Coming Soon!
Guidance Statements
(Back to top)
FDA Information Sheets
Human Subject Regulation Decision Charts
OHRP IRB Guidebook
OHRP Guidance by Topic
HIPAA
(Back to top)
45 CFR 160
Prisoners in Research
(Back to top)
Prisoners Involved with Research
Regulatory Guidance
(Back to top)
45 CFR 46
en español
21 CFR Part 50
21 CFR Part 54
21 CFR Part 56
21 CFR Part 312
21 CFR Part 314
21 CFR Part 812
38 CFR Part 16
Code of Federal Regulations
21 CFR Part 11
For CITI in Spanish:
CITI en español
Instrucion de CITI en español
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