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Suggested Reading
- AAPP (American Academy of Pharamceutical Physicians) — Devoted to the protection and welfare of patients in the discovery, development and use of new drugs.
- AAPS (American Association of Pharmaceutical Scientists)
- AACC (American Association for Clinical Chemistry)
- About Drug Studies — Sponsored by Feighner Research Institute.
- ACRP (Association of Clinical Research Professionals)
- Aegis Clinical Trials Knowledgebase
- AHRQ (Agency for Healthcare Research and Quality)
- ARENA (Applied Research Ethics National Association) — A national membership organization for professionals concerned with issues relating to: the protection of human subjects; the humane care and treatment of animals; scientific misconduct; ethical decision-making in healthcare; and other ethical issues pertaining to biomedical and behavioral research.
- Barnett International — Good review courses.
- BARQA (British Association of Research Quality Assurance) — Assuring good scientific practice in research and development.
- Belmont Report
- Belmont Report — Office of the Secretary; Ethical Principles and Guidelines for the Protection of Human Subjects of Research; the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research.
- BIO (Biotechnology Industry Organization)
- Bioethical Topics of Healthcare — Sponsored by the University of Washington School of Medicine
- Bioethics Resources on the Web
- Book: Women and Health Research: Ethical and Legal Issues
- BRANY (Biomedical Research Alliance of New York) Research Education
- Case Western Reserve University Center for Biomedical Ethics
- CCRP (Center for Clinical Research Practice) — Providing the foundation for excellence in clinical research through education, training, and ethical review.
- CDER Handbook of Drug Trials — Sponsored by the FDA.
- CenterWatch — Clinical trials listing service.
- CFR (Code of Federal Regulations), Title 45, Part 46, Protection of Human Subjects
- CFR from the US Government Printing Office/Federal Register
- CHR (Committee on Human Research)
- Clinical and Drug Trial Information
- Clinical Trials and Basic Research
- Clinical Trials Guide
- Clinical Trials Guide Picks
- ClinicalTrials.com
- Compassion vs. Control: When Should FDA Allow New Drug on Market?
- Cornerstone Institute — Education and training of clinical research professionals.
- Courses Sponsored by the Virginia Commonwealth University Medical College of Virginia
- Dartmouth College Sponsored Web Based Course
- Declaration of Helsinki
- Declaration of Helsinki from the World Medical Association
- Declaration of Helsinki — Recommendation for Conduct of Clinical Research
- Declaration of Helsinki — World Medical Association, Declaration of Helsinki; Ethical Principles for Medical Research Involving Human Subjects; first adopted by the WMA General Assembly, Helsinki, Finland, June 1964; last amended at the 52nd WMA General Assembly, Edinburgh, Scotland, October 2000
- DIA (Drug Information Association)
- Dictionary of Common Research Terms
- Drug Portal
- Duke University Web Based Research Course
- Education and Information Resources
- Ethical Conduct of Human Subject Research — A computer-based learning program for investigators, sponsored by Tulane University Medical Center.
- Ethical Issues in Research Involving Human Participants
- FAQ About Clinical Trials — Sponsored by CareInternet.net.
- FAQ About Clinical Trials — Sponsored by Northwest Gastroenterologists.
- FDA Information Sheets — Guidance for institutional review boards and clinical investigators.
- FDA List of Disqualified Clinical Investigators
- GCP (Good Clinical Practice)
- GCP Compliance: FDA Expectations and Recent Findings
- George Washington University Medical Center School of Medicine Sponsored Web Based Course
- GlaxoSmithKline Clinical Trials
- Glossary of Research Terms
- Good Clinical Practice in FDA-Regulated Clinical Trials
- Guinea Pigs Get Paid
- Harvard Sponsored Web Based Course
- Harvard/MGH-Institute of Health Professions Research Course
- Human Participants Protection Education for Research Teams — Sponsored by the NIH.
- Human Subject Protection and Financial Conflicts of Interest
- ICH (International Conference on Harmonization)
- ICH Technical Requirements for Registration of Pharmaceuticals for Human Use
- ICH-GCP Guidelines: Table of Contents
- IFAAP (International Federation of Associations of Pharmaceutical Physicians)
- IIRUSA (Institute for International Research, USA)
- Impact Consulting Group — Janet Zimmerman, MS, RN, has great GCP training
material
- Inclusion of Women and Minorities as Research Subject Volunteers
- Institutional Review Board For the Protection of Human Subjects in Research — University of Illinois at Urbana-Champaign.
- International GCP Regulations
- Introduction to Clinical Trials
- Johns Hopkins University Bioethics Institute
- Journal: Drugs in R&D
- Marshall University School of Medicine Clinical Drug Trials
- Master of Science in Clinical Research and Biostatistics — Medical College of Virginia.
- Medical College of Georgia — Web based review course.
- Medical College of Wisconsin — Web site on bioethics.
- National Patient Safety Foundation
- NIEHS (National Institute of Environmental Health Sciences)
- NIH Sponsored Web Based Review Course
- Nuremberg Code
- Nuremberg Code — Directives for human experimentation.
- Nuremberg Code of 1947 — Sponsored by CIRP.
- Nuremberg Trials Photo Gallery
- Nuremberg War Crimes and the Holocaust Memorial Museum
- Oath of Hippocrates, Circa 400 BC
- OBA (Office of Biotechnology Activities)
- OHRP (Office for Human Research Protections)
- Online Ethics Center
- Online Resources for Investigators Involved in Human Subject Research
- Online Resources for People Considering Participation in Research Studies
- ORI (Office of Research Integrity)
- Patient Clinical Trials Information
- Patient Info on Becoming a Research Subject Volunteer
- PERI (Pharmaceutical Education and Research Institute)
- PRIMR (Public Responsibility In Medicine and Research) — IRB aite affiliated with ARENA.
- PharmaLive — Pharmaceutical industry news.
- PharmWorld
- Phases of Alzheimers Drug Trials
- PhRMA (Pharmaceutical Research and Manufacturers of America)
- Protection of Human Subjects in Research Course — Sponsored by Indiana University.
- Questions Doctors Should Ask About Clinical Trials
- Questions Patients Should Ask About Clinical Trials
- RAN Institute — Dr. Nylen has excellent educational material for sale.
- RAPS (Regulatory Affairs Professional Society)
- RegSearch International
- RegSource.com — Information for regulatory affairs professionals.
- Research America — An Alliance for Discoveries in Health.
- Research Book by Yale University Press — Ethics and Regulation of Clinical Research.
- Research Practitioner — Published by the Center for Clinical Research Practice (CCRP).
- Research Training and Development
- Responsible Conduct of Research — The Regents of the University of California.
- Scope Clinical Research and Education Services
- SOCRA (Society Of Clinical Research Associates)
- Sponsor Search
- Testing Drugs in People — FDA special issue on new drug development.
- Training Program in Clinical Research by NIH and Duke
- TrialsCentral
- Understanding Clinical Research Drug Trials
- University of Texas M.D. Anderson Cancer Center Research
- University of Toronto, Canada, Research Web Site
- US Department of Health and Human Services (HHS)
- Veritas Medicine — About clinical trials.
- Virtual Pharmacy Center
- WOCBP (Women Of Child Bearing Potential) Ethical Issues

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