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Bioanalysis
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January 23, 2016
AAPS and US FDA Crystal City VI workshop on bioanalytical method validation for biomarkers
Steve Lowes, Bradley L Ackermann
Bioanalysis
|
November 19, 2010
Request for global harmonization of the guidance for Bioanalytical Method Validation and sample analysis
Philip Timmerman, Steve Lowes, Douglas M Fast, et al.
Bioanalysis
|
July 28, 2016
HRMS using a Q-Exactive series mass spectrometer for regulated quantitative bioanalysis: how, when, and why to implement
Robert M Sturm, Barry R Jones, Daniel E Mulvana, et al.
Bioanalysis
|
November 19, 2010
Building the Global Bioanalysis Consortium - working towards a functional globally acceptable and harmonized guideline on bioanalytical method validation
Peter van Amsterdam, Mark Arnold, Surendra Bansal, et al.
Bioanalysis
|
August 14, 2015
Scientific or regulated validation: a tiered approach? Meeting report from a joint EBF/DVDMDG workshop
Philip Timmerman, Steve Lowes, Stuart McDougall, et al.
The AAPS Journal
|
August 19, 2025
Case Studies on the Use of Patient-centric Sampling for Clinical Studies in Pharmaceutical Drug Development
Shefali Patel, Mike Baratta, Peter Bryan, et al.
The AAPS Journal
|
December 10, 2014
Implementing dried blood spot sampling for clinical pharmacokinetic determinations: considerations from the IQ Consortium Microsampling Working Group
Christopher Evans, Mark Arnold, Peter Bryan, et al.
Bioanalysis
|
November 19, 2010
2009 White Paper on recent issues in regulated bioanalysis from the 3rd Calibration and Validation Group Workshop
Natasha Savoie, Fabio Garofolo, Peter van Amsterdam, et al.
Bioanalysis
|
November 19, 2010
The 2nd Calibration and Validation Group workshop on recent issues in good laboratory practice bioanalysis
Natasha Savoie, Brian P Booth, Troy Bradley, et al.
The AAPS Journal
|
January 1, 2015
Workshop report: Crystal City V--quantitative bioanalytical method validation and implementation: the 2013 revised FDA guidance
Brian Booth, Mark E Arnold, Binodh DeSilva, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
Bioanalysis
|
January 23, 2016
AAPS and US FDA Crystal City VI workshop on bioanalytical method validation for biomarkers
Steve Lowes, Bradley L Ackermann
Bioanalysis
|
November 19, 2010
Request for global harmonization of the guidance for Bioanalytical Method Validation and sample analysis
Philip Timmerman, Steve Lowes, Douglas M Fast, et al.
Bioanalysis
|
July 28, 2016
HRMS using a Q-Exactive series mass spectrometer for regulated quantitative bioanalysis: how, when, and why to implement
Robert M Sturm, Barry R Jones, Daniel E Mulvana, et al.
Bioanalysis
|
November 19, 2010
Building the Global Bioanalysis Consortium - working towards a functional globally acceptable and harmonized guideline on bioanalytical method validation
Peter van Amsterdam, Mark Arnold, Surendra Bansal, et al.
Bioanalysis
|
August 14, 2015
Scientific or regulated validation: a tiered approach? Meeting report from a joint EBF/DVDMDG workshop
Philip Timmerman, Steve Lowes, Stuart McDougall, et al.
The AAPS Journal
|
August 19, 2025
Case Studies on the Use of Patient-centric Sampling for Clinical Studies in Pharmaceutical Drug Development
Shefali Patel, Mike Baratta, Peter Bryan, et al.
The AAPS Journal
|
December 10, 2014
Implementing dried blood spot sampling for clinical pharmacokinetic determinations: considerations from the IQ Consortium Microsampling Working Group
Christopher Evans, Mark Arnold, Peter Bryan, et al.
Bioanalysis
|
November 19, 2010
2009 White Paper on recent issues in regulated bioanalysis from the 3rd Calibration and Validation Group Workshop
Natasha Savoie, Fabio Garofolo, Peter van Amsterdam, et al.
Bioanalysis
|
November 19, 2010
The 2nd Calibration and Validation Group workshop on recent issues in good laboratory practice bioanalysis
Natasha Savoie, Brian P Booth, Troy Bradley, et al.
The AAPS Journal
|
January 1, 2015
Workshop report: Crystal City V--quantitative bioanalytical method validation and implementation: the 2013 revised FDA guidance
Brian Booth, Mark E Arnold, Binodh DeSilva, et al.
Page
of 3