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    • Clinical Trials
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Alliance for Human Research Protection
Alliance for Human Research Protection
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PDUFA

  • Gov. Medical Malfeasance

    GAO Report Gives FDA Flunking Grade in Detecting Drug Dangers

    April 24, 2006November 21, 2014

    “More than a year after the Food and Drug Administration announced it had strengthened its drug safety system, the agency still lacks a reliable system for keeping track of emerging problems, congressional investigators concluded in a report to be released today.” [Los Angeles Times, below]

    Read More GAO Report Gives FDA Flunking Grade in Detecting Drug DangersContinue

  • Business of Medicine

    Disease Mongering_Conference / PLoS Special Issue

    April 10, 2006November 21, 2014

    "Are we becoming patients for profit? That is the question knowledgeable observers are asking.

    Read More Disease Mongering_Conference / PLoS Special IssueContinue

  • FDA

    FDA Staff Travels on Drug Industry Dollars

    March 30, 2006November 21, 2014

    The Center for Public Integrity reports that FDA officials circumvent the prohibition on accepting trips from drug and medical device manufacturers.

    Read More FDA Staff Travels on Drug Industry DollarsContinue

  • Miscellaneous

    Big Pharma’s Shameful Secret

    November 2, 2005November 21, 2014

    "Every year, drug companies spend $14 billion to test experimental substances on humans. Across the U.S., the centers that do the testing–and the regulators who watch them–allow scores of human test subjects to be injured or killed."

    Read More Big Pharma’s Shameful SecretContinue

  • AHRP Testimonies

    Testimony of Meryl Nass, MD – Senate HELP Committee, Subcommittee on Bioterrorism

    February 8, 2005November 21, 2014

    Thank you for the opportunity to submit this testimony for the record.

    My name is Meryl Nass, M.D., and I have worked for the past twenty years as an emergency physician and internist in community hospitals in the northeastern US. I have also studied many aspects of bioterrorism since 1989. I am the person who first demonstrated, in 1992, that one could investigate an epidemic retrospectively, and prove that it was due to biological warfare, using Rhodesia’s 1978-80 anthrax epidemic as a model.[1]

    Read More Testimony of Meryl Nass, MD – Senate HELP Committee, Subcommittee on BioterrorismContinue

  • Presentations by AHRP/Board Members

    Conflicts of Interest in Clinical Trials

    May 7, 2002November 21, 2014

    Presented by Vera Hassner Sharav
    14th Tri-Service Clinical Investigation Symposium
    Sponsored by The U.S. Army Medical Department and The Henry M. Jackson Foundation for the Advancment of Military Medicine

    The cornerstone of public trust in medical research is the integrity of academic institutions and the expectation that universities, which rely on public funding, have a responsibility to serve the public good. Financial conflicts of interest affect millions of American people – those who are subjects of clinical trials testing new drugs and those who are prescribed drugs after their approval.

    Read More Conflicts of Interest in Clinical TrialsContinue

  • Miscellaneous

    Sharav Presentation before US Army Medical Dept., May 6, 2002

    May 5, 2002November 21, 2014

    CONFLICTS OF INTEREST Presented by Vera Hassner Sharav 14th TRI-SERVICE CLINICAL INVESTIGATION SYMPOSIUM Sponsored By THE U.S. ARMY MEDICAL DEPARTMENT And THE HENRY M. JACKSON FOUNDATION FOR THE ADVANCMENT OF MILITARY MEDICINE May 5-7, 2002 The cornerstone of public trust in medical research is the integrity of academic institutions and…

    Read More Sharav Presentation before US Army Medical Dept., May 6, 2002Continue

  • Miscellaneous

    InfoMail for March 8, 2002

    March 8, 2002November 21, 2014

      AHRP InfoMail Return to Home Page Return to InfoMail Media Coverage List MediaCoverage News Stories on Human ResearchProtection andCommentary by Vera Hassner Sharav March 8, 2002  FDA and Pharmaceutical Industry inPrivate Deal to Speed Drug Approval Process FYI According to the Washington Post, the FDA hasreached an agreement with the…

    Read More InfoMail for March 8, 2002Continue

  • Miscellaneous

    InfoMail for February 19, 2002

    February 19, 2002November 21, 2014

      AHRP InfoMail Return to Home Page Return to InfoMail Media Coverage List MediaCoverage News Stories on Human ResearchProtection andCommentary by Vera Hassner Sharav February 19, 2002 How a New FDA Policy Led toSeven Deadly Drugs FYI The Seattle Times reports, "Therelationship between the FDA and pharmaceutical industry changed fundamentallyunder former President…

    Read More InfoMail for February 19, 2002Continue

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  • Home
  • About
    • Board of Directors
    • Distinguished Advisory Board
    • Honor Role-Exemplary Professionals
  • Video
  • Support
  • Contact
  • All Articles
    • Medical Research Ethics
      • First, do no Harm
      • Human Rights
      • Informed Consent
      • Nuremberg Code
    • Eugenics / Bioethics
      • Discrimination
      • Medicalized Racism
      • Gene Modification
      • Depopulation
    • Corrupted Science
      • Scientism
      • Technocracy
      • Bias/Fraud
      • Propaganda — Censorship
      • Clinical Trials
      • Concealed Data
      • Public-Private Partnerships
      • Pharma Corrupt Influence
      • Publication Bias
    • Medical Atrocities
      • Organ Haversting
      • Bioweapon Experiments
      • Transhumanism
      • Current Medical Atrocities
      • Japanese Medical Atrocities
      • Nazi Medical Atrocities
      • Operation Paperclip
      • CIA Mind-Control
      • CIA Torture
      • U.S. Radiation Experiments
      • Unethical Experiments
    • Current Controversies
      • Pandemic Control
      • Great Reset
      • Digital ID
      • Apartheid Policies
      • Covid Pandemic
      • Epidemics
      • Government Overreach
    • Vaccine Controversies
      • Vaccine Profit Engine
      • Child Sacrifice
      • Vaccine mandates
      • Vaccine Risks
      • Vaccine Safety
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