|Year : 2013 | Volume
| Issue : 4 | Page : 203-209
Hippocratic oath and conversion of ethico-regulatory aspects onto doctors as a physician, private individual and a clinical investigator
Mohammed Imran1, Shadab Samad2, Mohammad Maaz3, Ashhar Qadeer4, Abul Kalam Najmi5, Mohammed Aqil6
1 Department of Pharmacology, Hamdard Institute of Medical Sciences and Research, New Delhi, India
2 Department of Medicine, Maulana Azad Medical College and LNJP Hospital, New Delhi, India
3 Department of Moalijat, Faculty of Pharmacy, Jamia Hamdard (Hamdard University), New Delhi, India
4 Department of Kulliyat, Faculty of Medicine, Faculty of Pharmacy, Jamia Hamdard (Hamdard University), New Delhi, India
5 Department of Pharmacology, Faculty of Pharmacy, Jamia Hamdard (Hamdard University), New Delhi, India
6 Department of Pharmaceutics, Faculty of Pharmacy, Jamia Hamdard (Hamdard University), New Delhi, India
|Date of Web Publication||27-Nov-2013|
Department of Pharmacology, Hamdard Institute of Medical Sciences and Research and Associated Hakeem Abdul Hameed Centenary Hospital, Jamia Hamdard, New Delhi -110 062
| Abstract|| |
Hippocratic Oath is a living document for ethical conduct of the physicians around the world. World Medical Association has been amending the oath as per the contemporary times. Although physicians maintain their ethical standards while treating a patient yet many a times social, administrative and ruling powers either use physicians as their tool of oppression or victimize them for conducting duties as per their oath. The Tuskegee Syphilis Study and Human Radiation Experiments in America, Nazi Experiments in Germany and compulsory sterilization program in India were the studies where States used physicians for the advancement of their rationality or belief. Conversely victimization of physicians in Kosovo, Sri Lanka and incarcerating physicians for treating human immunodeficiency virus/acquired immunodeficiency syndrome patients in some countries is concerning. The Nuremberg code, the Declaration of Geneva, Belmont Report and Declaration of Helsinki are ethical documents while active involvement of Food and Drug Administration through "common rule" resulted in guidelines like International Conference on Harmonization and Good Clinical Practices. Still unethical studies are found in developing countries. Studies such as experimental anticancer drugs in 24 cancer patients without adequate prior animal testing and informed consent in Kerala, studies at All India Institute of Medical Sciences in New Delhi resulted in 49 deaths of children and many more suspicious studies are rampant. Reverting back to the fundamentals of the medical profession; teaching medical ethics and enforcement of "medical neutrality" by embarking some grade of "medical immunity" on the basis of the oath is necessary for ethical conduct of physicians.
Keywords: Ethical documents, hippocratic oath, medical ethics, medical immunity, medical neutrality
|How to cite this article:|
Imran M, Samad S, Maaz M, Qadeer A, Najmi AK, Aqil M. Hippocratic oath and conversion of ethico-regulatory aspects onto doctors as a physician, private individual and a clinical investigator. J Mid-life Health 2013;4:203-9
|How to cite this URL:|
Imran M, Samad S, Maaz M, Qadeer A, Najmi AK, Aqil M. Hippocratic oath and conversion of ethico-regulatory aspects onto doctors as a physician, private individual and a clinical investigator. J Mid-life Health [serial online] 2013 [cited 2014 Nov 27];4:203-9. Available from: http://www.jmidlifehealth.org/text.asp?2013/4/4/203/122232
| Introduction|| |
Medical practitioners under oath who follow medical ethics must understand the word Ethics and derivation of its principles in medical practice over a period of time. Ethics refers to moral principles that control or influence a person's behavior whereas "ethical" means connected with beliefs and principles about what is right and wrong.  Origin of the word Ethics is from the Greek word "ethos" meaning custom or character. It exudes from within a person, imparts a value system distinguishing rights from the wrongs and build after imbibing values achieved from parents, religion, culture, society, faith and other influences. The principles of medical ethics have been penned down by many great physicians that affect every aspect of the medical professionals including their role as a physician as a private individual and as a clinical investigator.
| Doctors as a Physician|| |
It is quite obvious that out of these principles Hippocratic Oath [Table 1] is the most revered one. That is an old (460-377 BC), honored and living "ethical code" for physicians and a binding document for their conduct. , Its relevance has been increasing over the time especially in conflict areas of the world. The aftermath of the biggest conflict of the present century, i.e., World War II (WW2), revealed the reciprocal vulnerability of the doctors in a changing socio-administrative milieu. Moreover, the most famous trial of the physicians of the Nazi era for their atrocities on the minority was not held on the basis of then existing rules and laws of the Germany, but on the basis of Hippocratic Oath.  That implies that the professional ethical duties of doctors stand above the ruling powers and laws of the land. Most of the time oath takers are victimized for pursuing their duties as per their binding document. Recently, we witnessed that physicians had been killed in artillery attacks on hospitals and detained by the government in Sri Lanka in 2009  for treating the perceived adversaries of the state. The 34 Kosovar Albanian physicians were detained, tortured and killed extra-judicially by Serbian forces in conflict areas.  Treating patients of human immunodeficiency virus/acquired immunodeficiency syndrome (HIV/AIDS) may be considered a crime in some part of the world due to conflicting perception of the State and dilemma of the physicians in case of Intra or Intergenerational assisted reproduction has put another ethical dimension in exercising their duties.
|Table 1: Original oath translated by Michael North, national library of medicine, 2002|
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| Doctors as a Private Individual|| |
Despite the original Hippocratic Oath in its second paragraph denouncing the charging and fee taking culture in medical education and considering charging fee as a roadblock in delivering a free and fair health-care. The emerging issue that has infested the medical fraternity, now, is the commercialization of medical education and services. The large scale privatization of medical education in many countries has resulted in the lot of investment and expenditure in getting MBBS and a specialization degree. This creates an inherent individual self-interest in recovering the investment by unnecessary means of creating liaisons with pharmaceutical companies, diagnostic laboratories and charging the patients.
| Doctors as a Clinical Investigator|| |
By virtue of Hippocratic Oath all the physicians of the world are congregated into one global ethical community. However, their voices are not always shared as we find only few contributions on medical ethics discussion in the international medical literature from authors of developing countries.  Especially from India which is the hotbed for clinical trials activities as much as 20-30% of the global share.  There are many unethical clinical trials in India without any regulatory approval such as with Letrozole in 430 women for ovulation, customized erythromycin vaginal pellets in 790 impoverish women and an anticancer drug without any preclinical animal studies administered to 24 patients in Kerala.  This led John Hopkins University to make a conclusion that drugs with inadequate animal testing are being used in patients with inadequate informed consent and thus clinical investigators use patients as guinea pigs in them. 
Revisit and proper understanding of the Hippocratic Oath is very necessary in the light of present issues of ethical malpractices throughout the world. Consequently, Hippocratic tradition progression in the form of Modern version of oath by World Medical Association [Table 2] has shifted the benevolent paternalism of physicians toward empowerment of patients' decision making in Clinical Care and their rights in Clinical Research. , This drastic change of authority of decision making has led to the utmost consideration of values, preferences and decision making of the treating subjects.  Therefore, now there is a consensus in many parts of the world to teach medical ethics in graduate courses for high standards of personal and professional values and that the knowledge of the ethical and legal aspects of medicine is important for comprehensive health-care.  The current understanding of ethics in clinical care is the outcome of horrifying tragedies suffered by the mankind. 
|Table 2: Duties of Physicians adopted by the 3rd general assembly of the world medical association, London, England, october 1949 latest updated on 57th WMA general assembly, Pilanesberg, South Africa, october 2006|
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| Historical Perspective|| |
The dilemma of present medical practice is that the ethical principles for patient care, education and consent cannot be understood without the historical context of those horrifying tragedies  as Winston Churchill put it once "Those that fail to learn from history are doomed to repeat it". Moreover, doctors are even more vulnerable to fall in the hands of corrupt political and administrative regimes of the state.  Nazi experiments were the notorious highlight for the professional misconduct under a dictatorial regime.
There were many inhuman clinical trials on the Jews in WW2 like placing people in vacuum chambers to determine the high altitude effects of low pressure and oxygen and placing people in ice water for days without any food.  Experiments like sacrificing one of the twin brother or sister to compare the normal anatomy with the other where disease was induced to study the etiopathogenesis of natural history of the disease after autopsy of the dead one. 
The 20 Germen physicians convicted by American forces after WW2 asked the judiciary to try them on the basis of existing guidelines in their country "Guidelines for Human Experimentation of 1931," first of their kind, but this did not happen as The chief Prosecutor Brig. Gen Telford Taylor in his opening statement said that the defendant had violated the fundamental principle of Hippocratic Oath "Primum non nocere."  "The Nuremberg Code"  was framed and they were put on trial on four counts: (1) The common design or conspiracy, (2) war crimes, (3) crimes against humanity and (4) membership in a criminal organization. ,
It is not that doctors of the conflict zone become the tool of oppression in the hands of autocratic powers to conduct inhuman studies. Rather, a more stable society like United Stated of America had also been involved in violation of even the basic human rights. That is why it becomes imperative on every physician to read the new version of Hippocratic Oath and Declaration of Helsinki as these are the living ethical documents. 
The Tuskegee Syphilis Study  was started in 1932 as a 6 months study, even before the Nazi Experiments were conducted, by the United States Public Health Service department to study the natural history of Syphilis in around 400 black participants in Alabama, United States of America. The participants were given the impression that Government is giving them the free health-care, making it one of the earliest cases of "therapeutic misconception." It was neither conveyed to them what the disease is, nor treated with the penicillin, though the cure was widely available in 1951, nor stopped even when the "declaration of Helsinki"  was adopted in 1964. It was stopped when news published in the newspaper in New York Times in 1972 and treatment was given to the survivors in 1973, that is, almost 30 years after the Nazi Experiments.
The Willowbrook Viral Hepatitis study,  Obedience to Authority Study (Milgram Study)  and Monster Study  were the other horrifying studies. In first mentally challenged children were fed with the stool extract infected with hepatitis virus and later on, injected with purified viral preparations and were refused admission in institution meant for mentally retarded children if parents did not consented to the study, second study involved the administration of 450 v currents to the participants by deception to replicate the psychological affliction to obey orders and in third, 22 orphan children were put under tremendous negative psychological stress to convert their normal speech into stuttering.
Beecher, professor at Harvard University, reported in New England Journal of Medicine in 1966, about 22 out of 50 such unethical studies, which were being conducted in America like to determine whether central Nervous system or cardiovascular system would collapse first. It was carried out by reducing blood pressure of the participants from the mean of 109 mmHg to mean of 48 mmHg without even considering the hypoxic damage of the brain post experimentation; giving high diet of nitrogen to generate hepatic encephalopathy in patients of cirrhosis of liver; and patients with minor surgeries put under cyclopropane anesthesia monitored for development of cardiac arrhythmias with different concentrations of Carbon dioxide injected in closed respiratory system by endotracheal intubation. 
After president Bill Clinton formed the Advisory committee on "human radiation experiments" in 1994, it was revealed that US government had intentionally released radiation on many occasions from 1944 to 1974 and injected Plutonium in unaware subjects to see the effects of the atomic bomb on the people.  Many incidents of medical intervention were done by the doctors under coercion by the states in many of countries like "forced vasectomy" or also known as compulsory sterilization to reduce the growing human population specially that of minority community. It was aggressively followed in India where many coercive tactics were used by the Government during the 19 months of excesses of Emergency from 1976 to 1977  where approximately 8 million vasectomies were done which was total 4 times that of previous years and 8 times that of the period before that.  The weaknesses of the studies such as Women's Health Initiative hormone trials,  Death of Ellen Roche  and 49 deaths of babies in All India Institute of Medical Sciences (AIIMS)  have raised the concern of in competency of Institutional Review Board (IRB) and Independent Ethics Committee (IEC). Ellen Roche, an employee of the John Hopkins Asthma and Allergy Centre, was enrolled in the study of the same institute for inducing asthma by "hexamethonium" though it was not approved by Food and Drug Administration (FDA) as medication. Yet both National Institute of Health and the IRB had approved the study and she died. It came to light that Pediatrics department of AIIMS, India, vigorously conducted 42 sets of trials in 2½ years since January 1, 2006, to August 2008 where 49 babies died. It was seen that children of the poor families were kept for a long time in the hospital and the hospital, in reply to a query, justified that trials were conducted after clearance from their own ethics committee, the health ministry steering committee on ethics and the national ethics committee of Indian Council of Medical Research and Department of Biotechnology.
| Ethical Documents|| |
Almost all hospitals have physicians as part of the ethical committees. The practice of evidence based medicine and ethical conduct demands understanding of ethical and legal issues of the present time. The physicians maintain their conduct to the highest standards from the time of antiquity on the basis of dynamic changes in the Hippocratic Oath wherein modern time has seen huge scientific and social changes. The original version of the oath was lacking many newer issues such as different professional aspect of medical specialization, privacy of the patients and doctors' societal and legal responsibilities. The World Medical Association in its 2 nd general assembly modernized the oath in Declaration of Geneva in 1948 and the latest version was modified in 2006 in its 57 th General Assembly in South Africa to incorporate the changing aspects of medicine [Table 3]. 
The "Nuremberg code" was another milestone in Ethical documents for physicians after the conviction of Nazi doctors and it was built as regulatory guidelines for all the physicians of the world. Furthermore, it never got the acceptance for ethical conduct in the western world. The "declaration of Helsinki" was adopted in 1964 as the extension of Nuremberg code. Many new aspects were added in the Declaration where concept of legal guardianship was added for the consent for participation in clinical research in cases of legal incapacity. It also brought the concept of reviewing the research protocols by the independent committees.
|Table 3: Oath adopted by the 2nd General Assembly of the WMA, Geneva, Switzerland, September 1948 latest updated on the 173rd WMA Council Session, Divonne-les-Bains, France, May 2006|
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Although Declaration of Helsinki became the most important milestone for the ethical conduct of the physician, but, it was ignored in major developed countries like USA where Tuskegee Syphilis Study compelled the parliament to pass an Act in 1974, creating a National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. This commission produced a report called "Belmont report"  on the basis of principles of medical ethics introduced by Beauchamp and Childress in 1979  for the ethical treatment of human subjects that includes three major concepts. One is "respect for person," second "beneficence" and third was the "justice." The Belmont report became the reference document for IEC/IRB.
| Regulatory Outcomes|| |
Controlling the chain reactions started by distancing physicians from the basic tenants of Hippocratic Oath requires regulatory noose on clinical investigators. The regulation in the Clinical care and research all over the world follows the changes in FDA of USA,  which was enacted in 1906 as Pure Food and Drug Act basically to regulate the inter-state trade of misbranded and adulterated foods, drinks and drugs. The physicians were unaware of the adulteration of drugs and thus, a great tragedy occurred in 1938 in which almost 107 people died due to prescription of "Elixir Sulfanilamide" containing toxic ingredient "diethylene glycol," which is used as anti-freeze in biofuel. , The act was revised to Food, Drug and Cosmetic Act and it required a manufacturer to prove the safety of a drug before it could be marketed and later in 1962, when Kefauver-Harris Drug Amendments  was added after "thalidomide disaster" when a sedative drug thalidomide caused the seal like limb deformity (Phocomelia) in newborn babies and the "cutter incidents"  in 1955 where 40,000 children develop abortive polio, 51 permanently paralyzed, 10 died, including family members, after receiving vaccine containing live polio virus. The National research act of 1974 in USA also established the "common rule"  to protect the vulnerable subjects. These Codes of Federal Regulations control Pharmaceutical industry research through FDA. Although Clinical Research became very well-regulated affair in developed countries but developing countries were lacking the initiatives to frame the regulatory guidelines.
In 1982, a non-governmental organization, The Council for International Organization of Medical Sciences collaborated with the World Health Organization (WHO) and United Nations to translate the "declaration of Helsinki" into regulatory guide document for third world countries. It proposed "International Ethical Guidelines for Biomedical Research" involving human subjects later updated in 2002  when a controversy occurred in Africa about the intervention in treating HIV/AIDS patients for not maintaining "clinical equipoise." Later on it was seen that every country operates in a different set of technical and administrative milieu and even with extra and unnecessary efforts it was difficult to get the approval of redundant technical requirements therein.
The European Federation of Pharmaceutical Industries and Associations in 1990 arranged a meeting for regulatory and industry representative from USA, Japan and Europe to "harmonize" the regulatory requirements, overcoming the country specific hurdles. These meetings resulted in guidelines called "International Conference on Harmonization of Technical Requirements for Registration of Pharmaceutical for Human Use."  The most important outcome of these guidelines was the creation of "the Guidelines for Good Clinical Practices (GCP)" in 1996 containing, definitions of technical terms such as blinding, protocol and randomization, principles of GCP, vulnerable subjects, section of IRB including Informed Consent and distinction between IRB and IEC.
It is now being appreciated that legal, ethical and regulatory knowledge is essential for every practicing doctor to become a clinical investigator and simultaneously providing evidence based comprehensive therapy. Teaching of Ethics and Regulation is important for medical graduates in the present scenario. Oath bearers should be the trainers of oath takers to inculcate the professional ethics for right, safety and well-being of the patients throughout the teachings of medical graduates. Furthermore, it is imperative to involve the oath bearers for teaching the ethics, conducts the clinical research and become part of the various ethical and regulatory bodies. It will reduce difficulties faced by surrendering clinical research to people who are not oath-takers, do not care for patients and have little knowledge of conducting clinical trials.  Ethics of Clinical Care and Clinical Research are different and negates the very purpose of patient care if doctor views every patient as a potential subject as it violates the physicians' duty to provide most appropriate treatment.
In our opinion, contemporary churning phases of human lives all over the world where no one knows how many physicians are being compelled by the autocratic regime to do the anti-Hippocratic activities, some grade of "Medical Immunity" to oath takers should be there as a "Global community beyond the boundary of states." It should be at par like diplomatic immunity given to diplomats, to protect and maintain the medical neutrality affected by the political gains. Remedy of ethical malpractices, ameliorating conflict with the individual self-interest, maintaining medical neutrality and providing compassionate patient care can only happen if every physician trained on the basis of no-profit no-loss philosophy. Therefore rationing of health-care including training of medical professionals, empowerment of physicians as an autonomous entity related to the deliverance of their duty and adherence to their oath is paramount for their free and transparent obligation.
| References|| |
|1.||Hornby AS, Wehmeir S, McIntosh C, Turnbull J, Ashby M, editors. Oxford Advanced Learner′s Dictionary of Current English. Oxford: Oxford University Press; 2010. |
|2.||Markel H. "I swear by Apollo" - On taking the Hippocratic oath. N Engl J Med 2004;350:2026-9. |
|3.||Translation by North M. (US) National Library of Medicine. Available from: http://www.nlm.nih.gov/hmd/greek/greek_Oath.html. 2002. [Last accessed on 2012 Dec 4]. |
|4.||Ghooi RB. The Nuremberg code-A critique. Perspect Clin Res 2011;2:72-6. |
|5.||Selvakone M. Doctors in detention and the Hippocratic Oath. CMAJ 2009;181:E243. |
|6.||Physicians for human rights. Perilous medicine: The legacy of oppression and conflict on health in Kosovo, 2009. Available from: http://physiciansforhumanrights.org/library/reports/report-2009-06-16.html. [Last accessed on 2012 Sep 24]. |
|7.||Borry P, Schotsmans P, Dierickx K. Developing countries and bioethical research. N Engl J Med 2005;353:852-3. |
|8.||Bhatt A. Clinical trials in India: Pangs of globalization. Indian J Pharmacol 2004;36:207-8. |
|9.||Nundy S, Gulhati CM. A new colonialism? - Conducting clinical trials in India. N Engl J Med 2005;352:1633-6. |
|10.||Mudur G. Johns Hopkins admits scientist used Indian patients as guinea pigs. BMJ 2001;323:1204. |
|11.||World Medical Association. WMA International code of medical ethics, 2006. Available from: http://www.wma.net/en/30publications/10policies/c8/index.html.pdf">http://www.wma.net/en/30publications/10policies/c8/index.html.pdf. [Last accessed on 2012 Dec 04]. |
|12.||Truog RD. Patients and doctors - Evolution of a relationship. N Engl J Med 2012;366:581-5. |
|13.||Stirrat GM, Johnston C, Gillon R, Boyd K, Medical Education Working Group of Institute of Medical Ethics and Associated Signatories. Medical ethics and law for doctors of tomorrow: The 1998 consensus statement updated. J Med Ethics 2010;36:55-60. |
|14.||Fischer BA 4 th . A summary of important documents in the field of research ethics. Schizophr Bull 2006;32:69-80. |
|15.||Brandt AM. A reader′s guide to 200 years of the New England Journal of Medicine. N Engl J Med 2012;366:1-7. |
|16.||Hayward JS, Eckerson JD. Physiological responses and survival time prediction for humans in ice-water. Aviat Space Environ Med 1984;55:206-11. |
|17.||Seidelman WE. The professional origins of Dr. Joseph Mengele. CMAJ 1985;133:1169-71. |
|18.||Shuster E. Fifty years later: The significance of the Nuremberg code. N Engl J Med 1997;337:1436-40. |
|19.||Markman JR, Markman M. Running an ethical trial 60 years after the Nuremberg code. Lancet Oncol 2007;8:1139-46. |
|20.||Thatte U. Ethical issues in clinical research. In: Gupta SK, editor. Basic Principles of Clinical Research and Methodology. 1 st ed. New Delhi: Jaypee Brothers; 2007. p. 58-73. |
|21.||World Medical Association. Declaration of Helsinki-Ethical principles for medical research involving human subjects, 2008. Available from: http://www.wma.net/en/30 publications/10 policies/b3/index.html. [Last accessed on 2012 Sep 24]. |
|22.||Krugman S. The Willowbrook hepatitis studies revisited: Ethical aspects. Rev Infect Dis 1986;8:157-62. |
|23.||Cave E, Holm S. Milgram and Tuskegee - Paradigm research projects in bioethics. Health Care Anal 2003;11:27-40. |
|24.||Reynolds G. The stuttering doctor′s ′monster study′. N Y Times Mag 2003 Mar 16:4;36-9, 83-4. |
|25.||Beecher HK. Ethics and clinical research. N Engl J Med 1966;274:1354-60. |
|26.||Samei E, Kearfott KJ. A limited bibliography of the Federal Government-funded human radiation experiments. Health Phys 1995;69:885-91. |
|27.||Palmer ND. India in 1976: The policies of depolicization. Asian Surv 1977;17:160-80. |
|28.||Pandey GD, Pandey J. Attitude towards vasectomy during post-emergency period: A study of family welfare workers in Uttar Pradesh. POPCEN Newsl 1979;5:1-5, 16. |
|29.||Rossouw JE, Anderson GL, Prentice RL, LaCroix AZ, Kooperberg C, Stefanick ML, et al. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: Principal results from the women′s health initiative randomized controlled trial. JAMA 2002;288:321-33. |
|30.||Savulescu J, Spriggs M. The hexamethonium asthma study and the death of a normal volunteer in research. J Med Ethics 2002;28:3-4. |
|31.||Sinha K. 49 babies die during trials at AIIMS. The Times of India, 2008 Aug 18. Available from: http://timesofindia.indiatimes.com/articleshow/msid-3374492,flstry-1.cms.[Last accessed on 2013 Nov 08]. |
|32.||World Medical Association. Declaration of Geneva, 1948. Geneva, Switzerland: 2 nd General Assembly of the World Medical Association; 1948. Available from: www.wma.net/en/30publications/10policies/g1. [Last accessed on 2012 Sep 04]. |
|33.||National Commission for the Protection of Human Subjects of Biomedical and Behavioural Research. Ethics principles and guidelines for the protection of human subjects of research (aka the Belmont Report), 1979. Available from: http://ohsr.od.nih.gov/guidelines/belmont.html. [Last accessed on 2012 Nov 04]. |
|34.||Beauchamp TL, Childress J. The Principles of Biomedical Ethics. 6 th ed., Ch. 3. New York: Oxford University Press; 2008. |
|35.||Food and Drug Administration. U.S. Department of Health and Human Services. U.S. Food and Drug Administration. Available from: http: www.fda.gov/aboutfda/whatwedo/history/default.htm. [Last accessed on 2013 Aug 22]. |
|36.||Wax PM. Elixirs, diluents, and the passage of the 1938 federal food, drug and cosmetic act. Ann Intern Med 1995;122:456-61. |
|37.||Ritter JM. Drug regulation and therapeutic efficacy. Br J Clin Pharmacol 2008;65:801-2. |
|38.||Offit PA. The cutter incident, 50 years later. N Engl J Med 2005;352:1411-2. |
|39.||Department of Health and Human Services, National Institute of Health, Office for Protection from Research Risks. Title 45: Public welfare, Part 46: Protection of human subjects (aka the common rule), 2001. Available from: http://www.hhs.gov/ohrp/humansubjects/guidance/45cfr46.htm. [Last accessed on 2012 Nov 14]. |
|40.||Council for International Oraganisation of Medical Sciences. International ethical guidelines for biomedical research involving human subjects, 2002. Available from: http://www.cioms.ch. [Last accessed on 2012 Dec 04]. |
|41.||International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use steering committee. ICH harmonised tripartite guidelines, 1996. Available from: http://www.ich.org. [Last accessed on 2012 Nov 10]. |
|42.||Brown MJ. The impact of clinical trials legislation on clinical pharmacology: Problems and solutions. Br J Clin Pharmacol 2009;67:487-93. |
[Table 1], [Table 2], [Table 3]