Research Regulatory Compliance

Inbunden, Engelska, 2015

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Beskrivning

Research Regulatory Compliance offers the latest information on regulations and compliance in the laboratory. With the increasing complexity of regulations and need for institutional infrastructure to deal with compliance of animal use issues, as well as a requirement surrounding human subjects, this publication provides reputable guidance and information.

The book is extremely helpful as a resource for researchers, administrators, and technicians in the laboratory, and is also a great asset for faculty or new researchers coming in to the laboratory environment. It will help prepare users for the deluge of regulatory and compliance issues they will face while conducting their scientific programs.

The book is edited and authored by known leaders in the field of compliance and regulations, and contains extensive research on the topics. It represents the new standard for information in every laboratory.

Provides a "one-stop" , go-to resource for the many regulatory and compliance issues that affect laboratory study and research models
Extremely helpful as a resource for researchers, administrators, and technicians in the laboratory, and also a great asset for faculty or new researchers coming in to the laboratory environment
Focuses on United States regulations, covering both animal models and human subjects
Written and edited by known leaders in the field of regulatory compliance who bring many years of collective experience to the book

Produktinformation

Utgivningsdatum:2015-08-11
Mått:191 x 235 x 23 mm
Vikt:910 g
Format:Inbunden
Språk:Engelska
Antal sidor:344
Förlag:Elsevier Science
ISBN:9780124200586

Utforska kategorier

Medicinsk utrustning och medicinska tekniker inom Medicin

Mer om författaren

Mark A. Suckow is a private consultant in laboratory animal medicine and Professor (Emeritus) in Biomedical Engineering at the University of Kentucky where he previously served as Attending Veterinarian and Associate Vice President for Research. He received his DVM from the University of Wisconsin and subsequently completed a post-doctoral residency in laboratory animal medicine at the University of Michigan. Dr. Suckow has 35 years of experience in laboratory animal medicine, regulatory compliance, and animal facility management. With an interest in the use of animal models for cancer research, vaccinology, and biomaterials development, Dr. Suckow has published greater than 115 papers in refereed journals and has seven issued patents related to vaccine adjuvants and cancer vaccines. He has written or edited over 20 books on topics related to research and laboratory animal medicine. Further, he served as the 2006 President of the American Association for Laboratory Animal Science and the 2011 President of the American Society of Laboratory Animal Practitioners; and he currently serves as an emeritus member of the Council on Accreditation of AAALAC, International and as Editor in Chief for the Journal of the American Association for Laboratory Animal Science.

Innehållsförteckning

1. Human Subjects Research Protections 2. Investigational New Drug and Device Exemption Process 3. The Institutional Animal Care and Use Committee 4. Biological Hazards and Select Agents 5. Radiological Hazards and Lasers 6. Controlled Substances: Maintaining Institutional Compliance 7. Export Controls and US Research Universities 8. Data Management and Research Integrity 9. Intellectual Property 10. Financial Conflicts of Interest in Research 11. Good Laboratory Practices (GLPs) 12. Human Embryonic Stem Cell Research Oversight: A Confluence of Voluntary Self-Regulation and Shifting Policy Initiatives