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TAMBOLI TAMANNA N.
Department of pharmacology
M.PHARM First Year
Tatyasaheb Kore college of
Pharmacy
   In Apr Dr.Leo Alexander has submitted to the
    counsel for war Crimes six point defining
    legitimate medical research .
   The trial verdict adopted these point &added
    extra four point.
   The ten point constituted &called Nuremberg
    code.
   The Declaration of Helsinki & Nuremberg code
    are the basis for code of federal regulation .
   This regulation issued by the United state
    Department of health and human Services.
   The voluntary consent of human subject
   yield fruitful result for the good of society .
   designed &based on the result of animal experimentation
    &knowledge of natural history of the disease.
   conducted as to avoid all unnecessary physical ,mental
    suffering and injury.
   No expt. should be done when prior reason to death.
   Should give adequate facilities to protect the subject
   Expt. Conducted by only scientific qualified person.
   Subject should have liberty to bring the expt. at end when
    he suffer physical or mental injury continuation of expt. is not
    possible.
   Scientist must prepared to terminate the expt. At any stage.
   Degree of risk should never exceed that determined by
    humanitarian value .
 It adopted in June 1964 in
  helsinki, Finland and undergo
  six revision.
 It is the first significant effect of
  the medical community to
  regulate itself, form basis of
  most subsequent document.
   It Intended to be read as a whole each of its constituent paragraph.
   To promote safeguard the health of the patient.
   Primary purpose of medical research is to understand the cause,
    development, effect of disease, and improve ,prevention ,diagnosis .
   WMA encourages other participant involve in study.
   The research is evaluated for effectiveness, efficiency, accessibility
    and quality.
   Physician should consider the ethical, legal and regulatory norms
    and standard for research.
   No national or international ethical legal or regulatory requirement
    should reduce or eliminate any of the protection for research
    subject.
   Duty of physician is to protect the life,health,dignity,intigrity,privacy
    and confidentiality.
   The protocol should be clearly described .
   The research must provide monitoring information committee.
   Voluntaries should require supervision by qualified physician .
   Not allowed to reduce or eliminate any of protection for research .
   Scientific training &qualification require to individual.
   Physician must immediately stop a study when risk are outweigh the
    potential.
   Every precaution must be taken to protect privacy of research
    subject.
   Authors ,editors &publisher all have ethical obligation with regard to
    publication of result of research.
   Project is clearly described in research protocol .
   Research protocol must be submitted for consideration, comment
    guidance & approval to research ethics committee before study
    begin.
o   Syphilis is sexually transmitted disease causes infection
    by spirochete bacterium & transmitted by mother to
    fetus during pregnancy or birth
o   THE Tuskegee Syphilis studied by Fred D. Gray examines
    a medical study that occur in Tuskegee. He was the
    lawyer in the lawsuit against the government.
o      The main goal of this study was to seek out African
    American males in second stage of syphilis.
o   The test subject were told that they were receiving
    medical treatment for syphilis but in reality they never
    receive penicillin which was most effective treatment
    for syphilis.
o      After 40 years of race based experiment test subject
    realize that they had been involved in the exp. &not
    treated with medicine
o Grey wrote a book to explain the event of injustice
performed on the individual test subject & this is a example
of immorality

o Final settlement went in favor of prosecution, and they
were awarded with $10 million to split among the living
syphilitics and control ,and the relative of the deceased.

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Seminar

  • 1.
  • 2. TAMBOLI TAMANNA N. Department of pharmacology M.PHARM First Year Tatyasaheb Kore college of Pharmacy
  • 3.
  • 4. In Apr Dr.Leo Alexander has submitted to the counsel for war Crimes six point defining legitimate medical research .  The trial verdict adopted these point &added extra four point.  The ten point constituted &called Nuremberg code.  The Declaration of Helsinki & Nuremberg code are the basis for code of federal regulation .  This regulation issued by the United state Department of health and human Services.
  • 5. The voluntary consent of human subject  yield fruitful result for the good of society .  designed &based on the result of animal experimentation &knowledge of natural history of the disease.  conducted as to avoid all unnecessary physical ,mental suffering and injury.  No expt. should be done when prior reason to death.  Should give adequate facilities to protect the subject  Expt. Conducted by only scientific qualified person.  Subject should have liberty to bring the expt. at end when he suffer physical or mental injury continuation of expt. is not possible.  Scientist must prepared to terminate the expt. At any stage.  Degree of risk should never exceed that determined by humanitarian value .
  • 6.
  • 7.  It adopted in June 1964 in helsinki, Finland and undergo six revision.  It is the first significant effect of the medical community to regulate itself, form basis of most subsequent document.
  • 8. It Intended to be read as a whole each of its constituent paragraph.  To promote safeguard the health of the patient.  Primary purpose of medical research is to understand the cause, development, effect of disease, and improve ,prevention ,diagnosis .  WMA encourages other participant involve in study.  The research is evaluated for effectiveness, efficiency, accessibility and quality.  Physician should consider the ethical, legal and regulatory norms and standard for research.  No national or international ethical legal or regulatory requirement should reduce or eliminate any of the protection for research subject.
  • 9. Duty of physician is to protect the life,health,dignity,intigrity,privacy and confidentiality.  The protocol should be clearly described .  The research must provide monitoring information committee.  Voluntaries should require supervision by qualified physician .  Not allowed to reduce or eliminate any of protection for research .  Scientific training &qualification require to individual.  Physician must immediately stop a study when risk are outweigh the potential.  Every precaution must be taken to protect privacy of research subject.  Authors ,editors &publisher all have ethical obligation with regard to publication of result of research.  Project is clearly described in research protocol .  Research protocol must be submitted for consideration, comment guidance & approval to research ethics committee before study begin.
  • 10.
  • 11. o Syphilis is sexually transmitted disease causes infection by spirochete bacterium & transmitted by mother to fetus during pregnancy or birth o THE Tuskegee Syphilis studied by Fred D. Gray examines a medical study that occur in Tuskegee. He was the lawyer in the lawsuit against the government. o The main goal of this study was to seek out African American males in second stage of syphilis. o The test subject were told that they were receiving medical treatment for syphilis but in reality they never receive penicillin which was most effective treatment for syphilis. o After 40 years of race based experiment test subject realize that they had been involved in the exp. &not treated with medicine
  • 12. o Grey wrote a book to explain the event of injustice performed on the individual test subject & this is a example of immorality o Final settlement went in favor of prosecution, and they were awarded with $10 million to split among the living syphilitics and control ,and the relative of the deceased.