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Ethical Principles of Human Subjects Protection
The Belmont Report The Common Rule University of Pennsylvania School of Medicine
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University of Pennsylvania
The Belmont Report Purpose of the report is to provide three principles (prescriptive judgments) that will ‘assist researchers, subjects, reviewers and interested citizens with an understanding of the ethical issues inherent in HSR’ Statement consists of 3 parts Distinction between research and medical practice Establishment of 3 ethical principles Remarks regarding application of the principles University of Pennsylvania School of Medicine
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The Belmont Report Practice Research
Interventions designed solely to enhance the wellbeing of the patient and that have a reasonable expectation of success Research An activity designed to test an hypothesis, permit conclusions to be drawn, develop or contribute to generalizable knowledge
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The Belmont Report Three Ethical Principles
Principle of respect for persons autonomy Principle of beneficence Principle of justice
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Respect for Persons Autonomy
Enters research voluntarily and with adequate information Implies everyone is capable of self determination Matures during life span May be lost in whole or in part as a result of illness, mental disability or circumstances that restrict liberty Cannot exclude those incapable of self determination Respect for such situations requires protection Explicit requirement that each class of incompetent patient be considered on its own terms Third parties whose primary goal is to protect the subject from harm should be used and that these individuals be allowed to observe the research
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The Belmont Report - Three Ethical Principles
Principle of respect for persons Individual autonomy Protection of individuals with reduced autonomy Principle of beneficence Requires a risk benefit assessment be made Maximize benefits and minimize harms Principle of justice Equitable distribution of research costs and benefits
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Beneficence Acts of kindness or charity that go beyond strict obligation Strict sense of obligation Do not harm Maximize possible benefits Minimize possible harms Seek benefit despite certain risks Benefits should be forgone because of the risk
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The Belmont Report - Three Ethical Principles
Principle of respect for persons autonomy Principle of beneficence Requires a risk benefit assessment be made Principle of justice Fairness in selection of subjects Benefit is denied or burden is imposed
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How to Apply the 3 Principles
Autonomy - Informed consent Information Comprehension Voluntariness Beneficence – determination of the risk and benefits Peer review – risks are justified Investigator – study design Subject – the determination to participate Justice Selection of subjects described by the researcher Reviewed during the peer review process Determined to be equitable
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Pillars of Protection for Human Subjects Research
Consent Peer Review Research Integrity Conflict of Interest Disclose COI to employer, IRB, and subject COI committee Thresholds Management plan
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Pillars of Protection for Human Subjects Research
Consent Peer Review Research Integrity Duty to protect subjects Carry out studies per protocol Communicate with subjects Report findings honestly Conflict of Interest
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The Common Rule Further review by the president’s commission and other panels Mid 1980’s no standard government policy that coordinated the diverse regulations of all federal agencies 1986 the “Common Rule” proposed and then codified in 1991 Essentially identical to the 1981 DHHS policy CFR 46 Subpart A But by executive order extended that basic structure to the regulations of all 15 federal agencies and the CIA
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The Common Rule Comprehensive regulatory framework that formally governs all HSR conducted by the federal government or in facilities receiving federal funds Requires the establishment of a HSR Protection Program If meets the federal standard institutional assurance of compliance is issued Any institution that receives federal funding must have a Federalwide Assurance (FWA) Cert Mandates role of the IRB Defines requirements for informed consent Codifies special requirements for vulnerable populations
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THE COMMON RULE Additional Protections Included in 45 CFR 46 Subpart B
Additional Protections for Pregnant Women, Human Fetuses and Neonates Involved in Research (revised December 13, 2001) Subpart C Additional DHHS Protections Pertaining to Biomedical and Behavioral Research Involving Prisoners as Subjects Subpart D Additional DHHS Protections for Children Involved as Subjects in Research Note: Each agency decides which Subpart, if any, to adopt
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Basic Elements of a Program for Human Subject Protection in Research
NOTE: The Regulatory Sponsor is often the funding source, but not to be assumed Institution IRB Subject Investigator Regulatory Sponsor Funding Source Federal Agencies (FDA/OHRP)
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Human Subject Protection…
Sponsor IRB Institution Subjects Investigator Funding Federal Agencies
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Institution Responsibility
Protect the rights and welfare of research subjects Qualified IRBs appropriate to review research Human Protection Training HIPAA training Qualified administrative IRB support staff Operational space Budget to support the IRB operations Budget to support HSRP Program
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Investigator Responsibility
Protect the rights and welfare of research subjects Practice of ethics and professional standards appropriate to type of research Maintenance of IRB approval Adhere to protocol Comply with ALL applicable regulations Comply with ALL institutional requirements
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Subject Responsibility
Ask questions to obtain clear understanding of what is expected Comply with protocol requirements Report adverse events and unanticipated outcomes to investigator
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Responsibility of the Regulatory Sponsor
Protect the rights and welfare of research subjects Comply with ALL applicable regulations Provide data safety monitoring according to research risk level Appropriate safety reporting to IRB and associated regulatory agencies Ensure appropriate investigator/staff qualifications
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Responsibility of Funding Source
Protect the rights and welfare of research subjects Appropriate funding Ethical considerations Assurance from institution to comply with appropriate regulations
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Responsibility of Federal Agencies (FDA, OHRP, etc.)
Protect the rights and welfare of research subjects Ethical considerations Research approval Assurance from institution to comply with appropriate regulations Inspections of IRBs, Investigators and Sponsors Suspension or termination of research
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Responsibility of the IRB
Protect the rights and welfare of research subjects Oversight of the conduct of ALL human research Guidance and support to research staff through IRB review and administrative IRB support staff Ensures compliance with all federal, state, local and institutional requirements in human subject research
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3 Ethical Principles Autonomy - Informed consent
Information Comprehension Voluntariness Beneficence – determination of the risk and benefits Peer review – risks are justified Investigator – study design Subject – the determination to participate Justice Selection of subjects described by the researcher Reviewed during the peer review process Determined to be equitable
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Risk/Benefit Analysis
IRB Decision Matrix BENEFICENCE JUSTICE RESPECT FOR PERSONS Risk/Benefit Analysis Experimental Design Qualifications of PI Subject selection Inclusion/exclusion Recruitment The application of these general principles leads to the 3 requirements of informed consent, risk/benefit assessment and just selection of subjects for research. Privacy & Confidentiality Protection of subjects (especially vulnerable populations) Informed consent Surrogate consent Assent
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What does the IRB do? Approves or Disapproves “human research”
Requires modifications to approve “human research” Conducts continuing review and re-approval Observes/Monitors/Audits aspects of the research Suspends/terminates the research - initiated by Sponsor Investigator IRB
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What are the IRB regulations?
Title 45 of the Code of Federal Regulations, part 46 (45 CFR 46) Applies to all federally funded human research Includes federally funded research outside the US Title 21 of the Code of Federal Regulations, part 56 (21 CFR 56) Applies to all human research of FDA-regulated products Includes research outside the US conducted under an FDA filing IRB review is required of all human research Federally funded research Research involving FDA regulated products Research not federally funded or not involving FDA regulated products
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Which Regulations Apply and When?
FDA OHRP FDA: research involves products regulated by FDA Common Rule: Federally supported or conducted or conducted in an institution that agrees to review all research under the Common Rule Both: if Federally funded research involves FDA regulated product or FDA regulated research conducted in an institution that agrees to review all research under the Common Rule
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FDA REGULATIONS - Title 21
Parts 11 – Electronic records; electronic signatures 50 – Protection of Human Subjects 54 – Financial Disclosure by Clinical Investigators 56 – Institutional Review Boards 312 – Investigational New Drug 314 – New Drug Application 600 – Biological Products: General 812 – Investigational Device Exemptions 814 – Pre-market Approval of Medical Devices
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Your Responsibility as an Investigator
21 CFR 50 Informed Consent 56 IRB Regulations 54 Financial Disclosure 312 Investigational New Drug 314 New Drug Application 600 Biological Products 812 Investigational Device Exemptions 45 CFR Part 46 DHHS Human Subjects Regulations Social or scientific value Scientific validity Fair subject selection Favorable risk benefit ratio Independent review Informed consent Respect for autonomy
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