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Intentional human dosing studies for EPA regulatory purposes scientific and ethical issues by

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Published by National Academies Press in Washington, D.C .
Written in English

Subjects:

Places:

  • United States.

Subjects:

  • Human experimentation in medicine -- Moral and ethical aspects.,
  • Medicine -- Research -- Moral and ethical aspects.,
  • Human experimentation in medicine -- Government policy -- United States.,
  • Medical ethics.

Book details:

Edition Notes

Includes bibliographical references.

StatementCommittee on the Use of Third Party Toxicity Research with Human Research Participants, Science, Technology, and Law Program, Policy and Global Affairs Division, National Research Council of the National Academies.
ContributionsNational Research Council (U.S.). Policy and Global Affairs., National Research Council (U.S.). Committee on the Use of Third Party Toxicity Research with Human Research Participants.
Classifications
LC ClassificationsR853.H8 I575 2004
The Physical Object
Paginationxviii, 208 p. ;
Number of Pages208
ID Numbers
Open LibraryOL3382686M
ISBN 100309091721, 0309530989
LC Control Number2004556919
OCLC/WorldCa55880657

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The EPA commissioned The National Academies to provide advice on the vexing question of whether and, if so, under what circumstances EPA should accept and consider intentional humandosing studies conducted by companies or other sources outside the agency (so-called third parties) to gather evidence relating to the risks of a chemical or the conditions under . The committee decided that it could a provide a framework for clarifying some specific issues regarding the use of intentional human dosing studies for EPA regulatory decision-making purposes, but it made no pretense of being able to resolve all of the nettlesome issues, especially the potentially wide range of study-specific risk-benefit. Intentional Human Dosing Studies for EPA Regulatory Purposes: Scientific and Ethical Issues [National Research Council, Policy and Global Affairs, Technology, and Law Program Science, Committee on the Use of Third Party Toxicity Research with Human Research Participants] on *FREE* shipping on qualifying offers. The EPA commissioned The National . Get this from a library! Intentional human dosing studies for EPA regulatory purposes: scientific and ethical issues. [National Research Council (U.S.). Committee on the Use of Third Party Toxicity Research with Human Research Participants.; National Research Council (U.S.). Science, Technology, and Law Program.;].

Intentional Human Dosing Studies for EPA Regulatory Purposes: Scientific and Ethical Issues Committee on the Use of Third Party Toxicity Research with Human Research Participants Science, Technology, and Law Program, National Research Council. Genre/Form: Electronic books: Additional Physical Format: Print version: Intentional human dosing studies for EPA regulatory purposes. Washington, D.C.: National. Media Coverage. Intentional Human Dosing Studies for EPA Regulatory Purposes: Scientific and Ethical Issues () Read Online Free Buy the Book or Download the Free PDF. Janu WNCN Investigates: Alleged Conflicts of Interest in . Protection of Human Subjects in EPA's Research and Non-Research Studies Silver Cloud Hotel - Broadway Broadway Seattle, WA September 26 - 29, Agenda MONDAY, SEPTEM (DAY ONE) t PM Moderators: Roseanne Lorenzana and Barbara Lither - p.m. Sign-In at Workshop Registration Desk and Pick Up Meeting .

What types of human subjects research does EPA conduct and fund? EPA conducts and funds a wide variety of human subjects research (HSR). Some examples of HSR at the EPA include fish consumption surveys, surveys on household practices or demographics, analysis of biological specimens, use of focus groups, controlled exposure studies and epidemiology studies. See: “Department of Interior, Environment, and Related Agencies Appropriations Act, ,” Public Law ; and “Intentional Human Dosing Studies for EPA Regulatory Purposes,” Washington, DC: National Academy Press. Balanced membership will be driven by a number of considerations characterized by: inclusion of the necessary. Intentional Human Dosing Studies for EPA Regulatory Purposes by Policy and Global Affairs Division Staff; Use of Third Party Toxicity Research with Human Research Participants Science, Technology, and Law Program Committee (Contribution by); National Research Council (U.S) Staff; Science, Technology, and Law Program StaffAuthor: Rebekah McKinney. a recent us report may have wide-ranging impacts on international pesticide research and human health because it has given a clean chit to human testing of pesticides in the ional human dosing studies for epa regulatory purposes: scientific and ethical issues was drafted by the us National Academy of Sciences' Committee on the Use of Third Party Toxicity Research .