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Journal of Proteome Research
|
August 9, 2005
Introduction to the Food and Drug Administration (FDA) regulatory process
Joseph L Hackett, Steven I Gutman
The Journal of Molecular Diagnostics : JMD
|
February 1, 2005
Food and Drug Administration regulation of in vitro diagnostic devices
Elizabeth Mansfield, Timothy J O'Leary, Steven I Gutman
Diabetes Technology & Therapeutics
|
February 3, 2005
Consumers report glucose meter problems to FDA
Steven I Gutman, Janie G Fuller, Ethan D Hausman
Expert Review of Molecular Diagnostics
|
September 10, 2005
FDA perspectives on pharmacogenetic testing
Courtney C Harper, Reena Philip, Max Robinowitz, et al.
Human Genomics
|
February 8, 2006
FDA perspectives on potential microarray-based clinical diagnostics
Zivana Tezak, Daya Ranamukhaarachchi, Estelle Russek-Cohen, et al.
Journal of the National Cancer Institute
|
October 27, 2009
A perspective on challenges and issues in biomarker development and drug and biomarker codevelopment
Sheila E Taube, Gary M Clark, Janet E Dancey, et al.
Nature Genetics
|
November 28, 2002
Medical applications of microarray technologies: a regulatory science perspective
Emanuel F Petricoin, Joseph L Hackett, Lawrence J Lesko, et al.
Biosensors & Bioelectronics
|
February 14, 2006
Point-of-care biosensor systems for cancer diagnostics/prognostics
Steven A Soper, Kathlynn Brown, Andrew Ellington, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 18, 2014
Evidence of clinical utility: an unmet need in molecular diagnostics for patients with cancer
David R Parkinson, Robert T McCormack, Susan M Keating, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 22, 2017
The Role of Minimal Residual Disease Testing in Myeloma Treatment Selection and Drug Development: Current Value and Future Applications
Kenneth C Anderson, Daniel Auclair, Gary J Kelloff, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Journal of Proteome Research
|
August 9, 2005
Introduction to the Food and Drug Administration (FDA) regulatory process
Joseph L Hackett, Steven I Gutman
The Journal of Molecular Diagnostics : JMD
|
February 1, 2005
Food and Drug Administration regulation of in vitro diagnostic devices
Elizabeth Mansfield, Timothy J O'Leary, Steven I Gutman
Diabetes Technology & Therapeutics
|
February 3, 2005
Consumers report glucose meter problems to FDA
Steven I Gutman, Janie G Fuller, Ethan D Hausman
Expert Review of Molecular Diagnostics
|
September 10, 2005
FDA perspectives on pharmacogenetic testing
Courtney C Harper, Reena Philip, Max Robinowitz, et al.
Human Genomics
|
February 8, 2006
FDA perspectives on potential microarray-based clinical diagnostics
Zivana Tezak, Daya Ranamukhaarachchi, Estelle Russek-Cohen, et al.
Journal of the National Cancer Institute
|
October 27, 2009
A perspective on challenges and issues in biomarker development and drug and biomarker codevelopment
Sheila E Taube, Gary M Clark, Janet E Dancey, et al.
Nature Genetics
|
November 28, 2002
Medical applications of microarray technologies: a regulatory science perspective
Emanuel F Petricoin, Joseph L Hackett, Lawrence J Lesko, et al.
Biosensors & Bioelectronics
|
February 14, 2006
Point-of-care biosensor systems for cancer diagnostics/prognostics
Steven A Soper, Kathlynn Brown, Andrew Ellington, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 18, 2014
Evidence of clinical utility: an unmet need in molecular diagnostics for patients with cancer
David R Parkinson, Robert T McCormack, Susan M Keating, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
April 22, 2017
The Role of Minimal Residual Disease Testing in Myeloma Treatment Selection and Drug Development: Current Value and Future Applications
Kenneth C Anderson, Daniel Auclair, Gary J Kelloff, et al.
Page
of 1