Curtis Sheldon

Statistics

Publications

Citations

411

H-Index

Active since

2011

Affiliations

Pharmaceutical Product Development (United States)(Current)

Celerion (United States)

MPI Research (United States)

University of Colorado Colorado Springs

Worldwide Clinical Trials (United States)

Curtis Sheldon is an author at Pharmaceutical Product Development (United States) specializing in pharmacy, bioanalytical method validation, and assay validation.

Publications per year

2011–2023

Publications

Recommendations On: Internal Standard Criteria, Stability, Incurred Sample Reanalysis and Recent 483s by the Global CRO Council for Bioanalysis

Steve Lowes, Jim Jersey, Ronald E. Shoup et al. · Bioanalysis · 2011 · 88 citations

Pharmacy, Toxicology, Analytical Chemistry +13

Recommendations on The Interpretation of The New European Medicines Agency Guideline on Bioanalytical Method Validation By Global Cro Council For Bioanalysis (Gcc)

Mark Boterman, Mira Doig, Massimo Breda et al. · Bioanalysis · 2012 · 44 citations

Pharmacy, Pharmaceutical Analysis, Analytical Chemistry +15

Recommendations on Incurred Sample Stability (ISS) by GCC

Steve Lowes, Richard LeLacheur, Ronald E. Shoup et al. · Bioanalysis · 2014 · 34 citations

Pharmacy, Chemistry, Analytical Chemistry +16

Recommendations on Bioanalytical Method Stability Implications of Co-Administered And Co-Formulated Drugs By Global Cro Council For Bioanalysis (Gcc)

Steve Lowes, Mark Boterman, Mira Doig et al. · Bioanalysis · 2012 · 32 citations

Pharmacy, Pharmaceutical Analysis, Pharmacology +16

8th GCC: Consolidated Feedback to US FDA on The 2013 Draft FDA Guidance on Bioanalytical Method Validation

Joseph Bower, Douglas M. Fast, Fabio Garofolo et al. · Bioanalysis · 2014 · 31 citations

Pharmacy, Biomedical Sciences, Drug Approval Processes +14

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