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Thursday, July 30, 2020 | History

3 edition of Oversight hearing on implementation of NIH guidelines governing recombinant DNA research found in the catalog.

Oversight hearing on implementation of NIH guidelines governing recombinant DNA research

joint hearing before the Subcommittee on Health of the Committee on Labor and Public Welfare and the Subcommittee on Administrative Practice and Procedure of the Committee on the Judiciary, United States Senate, Ninety-fourth Congress, second session ... September 22, 1976.

by United States. Congress. Senate. Committee on Labor and Public Welfare. Subcommittee on Health.

  • 179 Want to read
  • 39 Currently reading

Published by U.S. Govt. Print. Off. in Washington .
Written in English

    Places:
  • United States.
    • Subjects:
    • DNA -- Research -- United States.,
    • Genetic recombination -- Research -- United States.

    • Edition Notes

      ContributionsUnited States. Congress. Senate. Committee on the Judiciary. Subcommittee on Administrative Practice and Procedure.
      Classifications
      LC ClassificationsKF26 .L354 1976j
      The Physical Object
      Paginationiv, 160 p. :
      Number of Pages160
      ID Numbers
      Open LibraryOL4689719M
      LC Control Number77601137

      NIH Recombinant DNA Advisory Committee (RAC)Advisory Committee (RAC) Federal advisory committee providing advice and recommendations to the NIH Director regarding recombinant DNA research Unique public forum for the discussion of science, safety, and ethics of recombinant DNA research Ri d l liil t fReviews and analyzes clinical gene transferFile Size: KB. Future Oversight of Recombinant DNA Research: Recommendations of an Institute of Medicine Committee Lawrence O. Gostin Georgetown University Law Center, [email protected] TheNationalInstitutesofHealth(NIH)establishedthe Recombinant DNA Advisory Committee (RAC) in

      a case analysis of nepa implementation: nih and dna recombinant research susan m. chalker* and robert s. catz** i. introduction ii. the national environmental policy act and dna recombinant research : Susan M. Chalker, Robert S. Catz. Seven types of risky studies would require approval by the Institutional Biosafety Committees that already oversee recombinant DNA research at some U.S. institutions. These “experiments of concern” include making an infectious agent more lethal and rendering vaccines powerless.

        Recombinant DNA Advisory Committee: Runtime: Description: The Recombinant DNA Advisory Committee is a federal advisory committee that provides recommendations to the NIH Director related to basic and clinical research involving recombinant or synthetic nucleic acid molecules. The Recombinant DNA Advisory Committee (RAC) advises the National Institutes of Health on the safe and ethical conduct of basic and clinical research involving recombinant DNA. It reviews protocols and provides recommendations for each protocol to .


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Oversight hearing on implementation of NIH guidelines governing recombinant DNA research by United States. Congress. Senate. Committee on Labor and Public Welfare. Subcommittee on Health. Download PDF EPUB FB2

Oversight hearing on implementation of NIH guidelines governing recombinant DNA research: joint hearing before the Subcommittee on Health of the Committee on Labor and Public Welfare and the Subcommittee on Administrative Practice and Procedure of the Committee of the Judiciary, United States Senate, ninety-fourth Congress, second session.

Oversight hearing on implementation of NIH guidelines governing recombinant DNA research: joint hearing before the Subcommittee on Health of the Committee on Labor and Public Welfare and the Subcommittee on Administrative Practice and Procedure of the Committee on the Judiciary, United States Senate, Ninety-fourth Congress, second session.

©— Bioethics Research Library Box Washington DC The guidelines, first published in (Recombinant DNA Research Guidelines, ) and amended through the years, have provided a comprehensive description of facilities and practices to prevent unintended release of or human exposure to genetically modified organisms and define the procedures for the RAC and outline requirements for research institutions' oversight Author: Rebecca N.

Lenzi, Bruce M. Altevogt, Lawrence O. Gostin. Research that involves testing in humans of materials containing recombinant or synthetic nucleic acids developed with NIH funds, if the institution that developed those materials sponsors or partic ipates in those projects.

A Brief History of Recombinant DNA Oversight. National Science Advisory Board for Biosecurity Report. National Science Advisory Board for Biosecurity (NSABB) chartered by U.S.

Government. Advisory to HHS Secretary, NIH Director, and heads of all Federal entities that conduct/support life sciences Size: KB. The NIH Guidelines Apply to Recombinant DNA research that isRecombinant DNA research that is Funded by the NIH Performed at or sponsored by an institution that receives any NIH funding for recombinant DNA research Rationale: For biosafety to be meaningful, it has to be observed by all investigators at an institution.

In addition, at present all researchers and institutions funded by the National Institutes of Health (NIH) are required by NIH guidelines to submit human gene transfer protocols for advisory review by the NIH Recombinant DNA Advisory Committee (RAC).

Some protocols are then selected for individual review and public by: Guide to the NIH Guidelines for Research Involving Recombinant DNA Molecules 3. Report any significant problems, violations of the NIH Guidelines, or research-related accidents or Investigate and report any significant problems pertaining to the operation and implementation of containment practices and procedures in writing to the Size: 82KB.

Forty years ago, NIH Director Robert S. Stone, M.D., established the Recombinant DNA Advisory Committee (RAC) to bolster oversight of the use of a new technology called recombinant DNA in research.

As the science evolved, so too did the role of the RAC which began considering gene transfer experiments in humans in the late s. regarding recombinant DNA research. A key role of the RAC is to advise the NIH Director and the NIH OBA, which is the NIH locus of oversight for recombinant DNA research.

In this capacity, the RAC recommends changes to the NIH Guidelines for Research Involving Recombinant DNA Molecules (NIH Guidelines), which. research. Appendix M sections M-III and M-IV were added to the NIH Guidelines for Research Involving Recombinant DNA Molecules (NIH Guidelines) to address points and issues related to informed consent that would benefit from particular attention.

These sections address issues unique to gene transfer, as well as issues that gene transfer has in. Recombinant DNA Registrations. The initiation of any experiment involving recombinant DNA (rDNA) molecules requires review by the NIH IBC.

PIs intending to work with rDNA must register their experiments through PI-Dashboard before experiments begin. The NIH IBC, whose functions are defined under the Guidelines. NIH Guidelines for Research Involving Recombinant DNA Molecules. Current information about the NIH Guidelines may now be found at the following URL: National Institutes of Health (NIH), Rockville Pike, Bethesda, Maryland.

NIH Guidelines for rDNA. Compliance with the NIH Guidelines for Research Involving Recombinant DNA Molecules is mandatory for every institution that receives NIH funding for research involving recombinant DNA (rDNA).

It is the responsibility of the Principal Investigator (PI) to make sure that his/her laboratory is in compliance. Following two scientific conferences at Asilomar, California, the National Institutes of Health moved quickly to create the Recombinant DNA Advisory Committee (RAC).

For approximately 38 years the RAC has served as an open forum for review of various recombinant DNA experiments, and for the last 23 years it has played a pivotal role in the oversight of human gene by: 9. If the protocol does involve the use of recombinant DNA then the research is covered under III-Da.

All experiments involving the use of other transgenic animals at any Biosafety Level and the use of transgenic rodents requiring BL2 or higher containment.

The NIH System in Retrospect Our oversight system, with local review as a pivotal element, has provided scientifically-based surveillance of this research that has Helped preserve public trust, and thus Permitted the science to move forward safely and in an informed manner Many lines of recombinant DNA research continue to raise many safety, ethical, and scientific issues.

Recombinant DNA Advisory Committee (RDAC): Developments at national and international levels in Biotechnology Currentness of the safety regulation for India on recombinant research use and applications To evolve long term policy for research and development in Recombinant DNA research. To formulate the safety guidelines for Recombinant DNA Research to be followed in India.

To recommended type of training programme for technicians and research fellows. Appendix M of these guidelines addresses oversight of such research by IBCs and IRBs, among other parties including the Recombinant DNA Advisory Committee (RAC), an advisory committee to the National Institutes of Health.

The process of RAC review has changed several times through the years. This chapter presents recombinant DNA guidelines and legislation.

In most of Western Europe, new legislation is not being contemplated; existing voluntary systems are considered perfectly adequate.

The revision of the NIH Guidelines for recombinant DNA has had great influence and for the smaller countries, the NIH model is easier to follow than Author: J.

Tooze.Title(s): Oversight hearing on implementation of NIH guidelines governing recombinant DNA research: joint hearing before the Subcommittee on Health of the Committee on Labor and Public Welfare and the Subcommittee on Administrative Practice and Procedure of the Committee of the Judiciary, United States Senate, ninety-fourth Congress, second session.Within the entire gene transfer research oversight system, the RAC is the only oversight or regulatory body that provides a public venue for the review of a protocol.

FDA, IRBs, and IBCs all convene in private; however, IRBs and IBCs often include .