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Cover of Guidelines for the Humane Transportation of Research Animals

Guidelines for the Humane Transportation of Research Animals

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Washington (DC): National Academies Press (US); .
ISBN-10: 0-309-10110-7

Excerpt

Over the last 10 years, the biomedical research enterprise has undergone tremendous growth. The amount of federal funding for biomedical research has more than doubled since 1995, and the pharmaceutical, biotechnology, and contract research sectors have all seen double-digit growth (PhRMA, 2005). That growth has been accompanied by parallel increases in research infrastructure, including an increase in the numbers of animals used in biomedical research. The humane transportation of research animals has been a priority, but there are concerns that the rapid increase in the numbers of animals transported, the increasing use of genetically modified animals that may have medical considerations, the complexity of permitting and inspection of research animals, and the dwindling availability of transportation services are adversely affecting the quality and ease of transportation in the United States.

Because of those concerns, the National Center for Infectious Diseases of the Centers for Disease Control and Prevention (CDC) and the National Institutes of Health asked the Institute for Laboratory Animal Research of the National Research Council to convene a committee to address problems associated with the transportation of research animals. The detailed charge to the committee is as follows: A committee will be formed to address current problems encountered in the transportation of research animals and make recommendations to rectify these problems to the benefit of the research community and the animals themselves. The committee will focus on all species used in biomedical research and all possible modes of transportation. Specifically, they will address: animal welfare concerns during transportation; availability of quality transportation services for animals, or lack thereof; overlaps or gaps in regulatory oversight; permitting issues; transportation of tissues/specimens; regulatory burden reduction; and potential biosecurity concerns.

Contents

This study was supported by the Elizabeth R. Griffin Research Foundation, the National Center for Infectious Disease, and Contract No. N01-OD-4-2139, Task Order 118 between the National Institutes of Health and the National Academy of Sciences. Any opinions, findings, conclusions, or recommendations expressed in this publication are those of the authors and do not necessarily reflect the views of the organizations or agencies that provided support for the project.

NOTICE: The project that is the subject of this report was approved by the Governing Board of the National Research Council, whose members are drawn from the councils of the National Academy of Sciences, the National Academy of Engineering, and the Institute of Medicine. The members of the committee responsible for the report were chosen for their special competences and with regard for appropriate balance.

The content of this publication does not necessarily reflect the views or policies of the National Institutes of Health, nor does mention of trade names, commercial products, or organizations imply endorsement by the US government.

The Internet information and government forms referenced in this report were correct, to the best of our knowledge, at the time of publication. It is important to remember, however, the dynamic nature of the Internet. Resources that are free and publicly available one day may require a fee or restrict access the next, and the location of items may change as menus and homepages are reorganized.

Copyright © 2006, National Academy of Sciences.
Bookshelf ID: NBK19637PMID: 20669437
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