Resources

E-Books

• Teaching the Responsible Conduct of Research in Humans
  Dr. Stanley Korenman in collaboration with the HHS Office of Research Integrity

Educational Sessions

• Bi-weekly sessions on internal policies, call x3054 to schedule
• Study Start Up Educational Sessions, call x8802 or x7555 to schedule
• IRB Packet Assembly, call x1019 to schedule
• Brown Bag Lunch Series, call x8802 or x7555 to register or with ideas, suggestions 
• Tutorial on Privacy vs. Confidentiality (powerpoint / developed by Joan Seiber)

Workshops/Conferences

• Emerging Issues & Ethics In Medicine  April 11, 2008, Storrs Campus

Monthly Newsletter

• January/February/March 2008
• October/November/December 2007
• July/August/September 2007
• April/May/June 2007
• January/February/March 2007
• November/December 2006
• September/October 2006
• July/August 2006
• May/June 2006
• March/April 2006
• January/February 2006
• December 2005
• November 2005
• October 2005
• September 2005
• August 2005
• July 2005
• June 2005
• May 2005

News Articles

April 2006

• Amgen
• London Trial Disaster 1
• London Trial Disaster 2

Books on Loan from the HSPO

• The CRC's Guide to Coordinating Clinical Research, Karen E. Woodin, Ph.D.
• The CRA's Guid to Monitoring Clinical Research, Karen E. Wooding, Ph.D. and John C. Schneider
• Protecting Study Volunteers in Research, A Manual for Investigative Sites, Cynthia McGuire Dunn, M.D. and Gary L. Chadwick, Pharm.D., MPH, CIP
• Becoming a Successful Clinical Research Investigator, Dr. David Ginsberg
• A Guide to Patient Recruitment and Retention, Diana L. Anderson, Ph.D.
• Institutional Review Board Member Handbook, Robert Amdur M.D., 2003
• Classics in Medical Literature, Medical Ethics or a Code of Institutes and Precepts Adapted to the Professional Conduct of Physicians and Surgeons, Thomas Percival M.D., 1803
• Responsible Research, A systems Approach to Protecting Research Participants, Institute of Medicine, 2003
• Creating an Ethical Framework for Studies That Involve the Worker Community, Prepared by Human Subjects Research Program, Office of Biological and Environment Research, Office of Science, U.S. Dept. of Energy
• Ethical and Policy Issues in Research Involving Human Participants, Volume 1, Reports and Recommendations of the National Bioethics Advisory Commission, 2001

Compact Discs on Loan from the HSPO

• Database Privacy - Coping with the HIPAA Privacy Rule on Research Databases and Tissue Repositories, Sponsored by Health Information Privacy Alert, 2/19/2004 (audio only)
• Investigator 101, Training for Investigators in the Responsible Conduct of Human Subjects Research, Public Responsibility in Medicine and Research (PRIM&R), 2001
• 2003 Annual Institutional Review Board (IRB) Conference, Sponsored by Public Responsibility in Medicine and Research, Applied Research Ethics National Association, Boston University School of Medicine.

To borrow any of the above items, contact Deb Gibb at 860-679-3054.

On-Line Resources

• American Medical Association
• Association for the Accreditation of Human Research Protection Programs
• Center for Devices and Radiological Health/Investigational Device Exemptions
• Center for Drug Evaluation & Research/IND Information
• Clinical Trials Network - Best Practices  
• Council for International Organizations of Medical Sciences
• Declaration of Helsinki
• Department of Health and Human Services
• Department of Health and Human Services/HIPAA
• Education Modules on Genetics Research Ethics (Duke)
• Ethics - Belmont Report
• Ethics (Code of) for National Association of Social Workers
• Ethics (Code of) for Sociologists
• Ethics (Code of) for Psychologists and Code of Conduct 
• Ethics - The Hastings Center
• Ethics - Kennedy Institute of Ethics Journal
• Ethics - Pharmaceutical Issues
• Ethics - President's Council on Bioethics
• Ethics Resources
• Federal Regulations/retrieval of
• Federal Regulations - The Common Rule and Subparts B, C and D
• Food and Drug Administration (FDA)
• FDA regulations for  Protection of Human Subjects
• FDA regulations for Institutional Review Boards
• FDA regulations for Investigational New Drugs
• FDA regulations for Investigational Device Exemptions
• FDA regulations for Humanitarian Use Devices
• Genome-wide Association Studies
• Good Clinical Practice/Consolidated Guidance
• Good Clinical Practice in FDA-Regulated Clinical Trials
• Hastings Center
• Health Insurance Portability and Accountability Act (HIPAA) Privacy Regulations
• Human Research Report
• International Conference on Harmonisation
• IRB Forum
• National Institutes of Health
• Office of Extramural Research/Certificates of Confidentiality
• Office for Human Research Protections
• Office of Research Integrity
• Public Act No. 05-149 Permitting Stem Cell Research
• Public Responsibility in Medicine and Research
• Research Advocacy Network
• Research Practitioner
• Translation Services - Global Language Solutions
• Translation Services - The Language Link of CT
• Translation Services - UMass Translation Center 
• World Health Organization
• World Medical Association