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Investigational device exemptions manual / prepared by Office of Health and Industry Programs, Division of Small Manufacturers Assistance ; project officers, James Park, Marsha Melvin, Althea Barcome. (HHS publication ; (FDA) 96-4159) (Medical devices)
Investigational device exemptions manual / prepared by Office of Health and Industry Programs, Division of Small Manufacturers Assistance ; project officers, James Park, Marsha Melvin, Althea Barcome. (HHS publication ; (FDA) 96-4159) (Medical devices)
Paper
図書
U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health
[1996]
<AU-541-A160>
National Diet Library
New drug approval process : clinical and regulatory management / edited by Richard A. Guarino. (Drugs and the pharmaceutical sciences ; v. 30)
New drug approval process : clinical and regulatory management / edited by Richard A. Guarino. (Drugs and the pharmaceutical sciences ; v. 30)
Paper
図書
Dekker
c1987.
<SD61-A6>
National Diet Library
Subject Heading
...United States.
Clinical Trials -- standards -- United States.
Drug Evaluation -- standards ...
Clinical research monitor handbook : GCP tools and techniques
Clinical research monitor handbook : GCP tools and techniques
Paper
図書
Deborah Rosenbaum, Fred Smith
Interpharm Press
c1998
Other Libraries in Japan
New drug approval process : clinical and regulatory management
New drug approval process : clinical and regulatory management
Paper
図書
edited by Richard A. Guarino
Dekker
c1987
Other Libraries in Japan
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