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Books Books 31 - 40 of 45 on US Department of Health and Human Services Food and Drug Administration Center for....
" US Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER... "
The Last Normal Child: Essays on the Intersection of Kids, Culture, and ... - Page 146
by Lawrence H. Diller - 2006 - 150 pages
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Molecular Genetic Testing in Surgical Pathology

John D. Pfeifer - Medical - 2006 - 474 pages
...archival material using fluorescence in situ hybridization. Oncogene 1996:13:63-72. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research. Oncology Drugs Advisory Committee, 58th Meeting, September 2, 1998. PM session: Biologies license application...
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Forecasting the in Vivo Performance of Modified Release (MR) Dosage Forms ...

Matthias Fischbach - 2006 - 296 pages
...(1997). SUPAC-MR: Modified Release Solid Oral Dosage Forms. Rockville, MD, US Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER). Guidance for Industry (1999). "Waiver of in vivo bioequivalence studies for immediate release...
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Drug Discovery and Development, Volume 1: Drug Discovery

Mukund S. Chorghade - Science - 2006 - 456 pages
...Chem., 1995, 32, 259-263. 12. Grozinger, KG; Hargrave, KD; Adams, JUS patent 5,571,912, 1996. of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine (CVM), February 2001. 14. (a) Wu, JC; Warren, TC; Adams, J.;...
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Fundamentals of Early Clinical Drug Development: From Synthesis Design to ...

Ahmed F. Abdel-Magid, Stéphane Caron - Science - 2006 - 400 pages
...Modified Release Solid Oral Dosage Forms: Manufacturing Equipment Addendum, US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), January 1999 (CMC 9, Revision 1). 36. Perry's Chemical Engineers' Handbook, 7th edition, Green,...
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Age Matters: Realigning Feminist Thinking

Toni M. Calasanti, Kathleen F. Slevin - Social Science - 2006 - 353 pages
...Clinical Development of Drug Trials for Treatment, Draft Guidance. Washington, DC: US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research. Foucault, M. (1980) The History of Sexuality Vol. I: An Introduction, trans. Robert Hurley. New York:...
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Addiction Treatment: Science and Policy for the Twenty-first Century

Jack E. Henningfield, Patricia B. Santora, Warren K. Bickel - Law - 2007 - 221 pages
...Information; Availability. Docket 2005D-0062, Federal Register 70 (89): 24606-607. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, Center for Biologics Evaluation and Research. 2000. Guidance for Industry. Recommendations for Complying...
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Analysis of Cosmetic Products

Amparo Salvador, Alberto Chisvert - Technology & Engineering - 2011 - 506 pages
...Toxicology 125, 149. US FDA, 2003, Guidance for Industry — Photosafety Testing. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Rockville (USA). Vohr H.-W., J. Bliimel, A. Blotz, B. Homey and HJ Ahr, 2000, Arch. Toxicol....
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Drug and Biological Development: From Molecule to Product and Beyond

Ronald Evens - Medical - 2007 - 383 pages
...dose in initial clinical trials for therapeutics in adult healthy volunteers. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, July 2005 13. US Food and Drug Administration (CDER). Guidance for Industry, Investigators, and Reviewers:...
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Understanding Drug Release and Absorption Mechanisms: A Physical and ...

Mario Grassi, Gabriele Grassi, Romano Lapasin, Italo Colombo - Medical - 2006 - 648 pages
...Addressing the solubility/permeability paradigm, Pharm. Tech., 22, 68, 1998. 2. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate-Release Solid Oral Dosage...
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Principles and Practice of Clinical Research

John I. Gallin, Frederick P Ognibene - Medical - 2011 - 448 pages
...hepatitis C. Consensus Interferon Study Group. Hepatology 1999;30: 787-793. 66. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Biologies Evaluation and Research (CBER), Center for Devices and Radiologie Health...
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