Workshop Report: AAPS Workshop on Method Development, Validation, and Troubleshooting of Ligand-Binding Assays in the Regulated Environment
暂无分享,去创建一个
Binodh DeSilva | Viswanath Devanarayan | Lauren Stevenson | Brian Booth | Marian Kelley | Sherri Dudal | Michaela Golob | Rand Jenkins | Eric Wakshull | Joao Pedras-Vasconcelos | Roland F. Staack | Ronald Bowsher | Marie Rock
[1] John W. A. Findlay,et al. Appropriate calibration curve fitting in ligand binding assays , 2007, The AAPS Journal.
[2] Binodh DeSilva,et al. Key elements of bioanalytical method validation for macromolecules , 2007, The AAPS Journal.
[3] Heather Myler,et al. Bioanalytical Approaches to Quantify “Total” and “Free” Therapeutic Antibodies and Their Targets: Technical Challenges and PK/PD Applications Over the Course of Drug Development , 2011, The AAPS Journal.
[4] Surinder Kaur,et al. Recommendations for Validation of LC-MS/MS Bioanalytical Methods for Protein Biotherapeutics , 2014, The AAPS Journal.
[5] Roland F Staack,et al. Mathematical simulations for bioanalytical assay development: the (un-)necessity and (im-)possibility of free drug quantification. , 2012, Bioanalysis.
[6] Eric Woolf,et al. Workshop Report: Crystal City V—Quantitative Bioanalytical Method Validation and Implementation: The 2013 Revised FDA Guidance , 2014, The AAPS Journal.
[7] Binodh DeSilva,et al. Recommendations for the Bioanalytical Method Validation of Ligand-Binding Assays to Support Pharmacokinetic Assessments of Macromolecules , 2003, Pharmaceutical Research.
[8] Roland F Staack,et al. Free analyte QC concept: a novel approach to prove correct quantification of free therapeutic protein drug/biomarker concentrations. , 2014, Bioanalysis.