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Journal of Drug Assessment
|
October 10, 2022
Investigation of potential substandard dry powder inhalers on EU and North African markets - evaluation of the delivered and fine particle doses
Yue Zhang, Philippe Hubert, Cédric Hubert
Journal of Pharmaceutical and Biomedical Analysis
|
August 27, 2018
Risk-based approach for method development in pharmaceutical quality control context: A critical review
Riccardo Deidda, Serena Orlandini, Philippe Hubert, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
December 5, 2021
Generic SFC-MS methodology for the quality control of vitamin D<sub>3</sub> oily formulations
Hugues Jambo, Amandine Dispas, Cédric Hubert, et al.
Molecules (Basel, Switzerland)
|
February 25, 2023
Quantitative Structure Retention-Relationship Modeling: Towards an Innovative General-Purpose Strategy
Priyanka Kumari, Thomas Van Laethem, Philippe Hubert, et al.
Data in Brief
|
March 21, 2022
A pharmaceutical-related molecules dataset for reversed-phase chromatography retention time prediction built on combining pH and gradient time conditions
Thomas Van Laethem, Priyanka Kumari, Philippe Hubert, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
July 24, 2024
Uncertainty management for In Silico screening of reversed-phase liquid chromatography methods for small compounds
Thomas Van Laethem, Priyanka Kumari, Bruno Boulanger, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
September 9, 2023
A multi-target QSRR approach to model retention times of small molecules in RPLC
Priyanka Kumari, Thomas Van Laethem, Diane Duroux, et al.
Molecules (Basel, Switzerland)
|
December 11, 2022
User-Driven Strategy for In Silico Screening of Reversed-Phase Liquid Chromatography Conditions for Known Pharmaceutical-Related Small Molecules
Thomas Van Laethem, Priyanka Kumari, Bruno Boulanger, et al.
Journal of Chromatography. A
|
April 11, 2007
Analysis of recent pharmaceutical regulatory documents on analytical method validation
Eric Rozet, Attilio Ceccato, Cédric Hubert, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
June 25, 2018
Implementation of a generic SFC-MS method for the quality control of potentially counterfeited medicinal cannabis with synthetic cannabinoids
Hugues Jambo, Amandine Dispas, Hermane T Avohou, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Journal of Drug Assessment
|
October 10, 2022
Investigation of potential substandard dry powder inhalers on EU and North African markets - evaluation of the delivered and fine particle doses
Yue Zhang, Philippe Hubert, Cédric Hubert
Journal of Pharmaceutical and Biomedical Analysis
|
August 27, 2018
Risk-based approach for method development in pharmaceutical quality control context: A critical review
Riccardo Deidda, Serena Orlandini, Philippe Hubert, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
December 5, 2021
Generic SFC-MS methodology for the quality control of vitamin D<sub>3</sub> oily formulations
Hugues Jambo, Amandine Dispas, Cédric Hubert, et al.
Molecules (Basel, Switzerland)
|
February 25, 2023
Quantitative Structure Retention-Relationship Modeling: Towards an Innovative General-Purpose Strategy
Priyanka Kumari, Thomas Van Laethem, Philippe Hubert, et al.
Data in Brief
|
March 21, 2022
A pharmaceutical-related molecules dataset for reversed-phase chromatography retention time prediction built on combining pH and gradient time conditions
Thomas Van Laethem, Priyanka Kumari, Philippe Hubert, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
July 24, 2024
Uncertainty management for In Silico screening of reversed-phase liquid chromatography methods for small compounds
Thomas Van Laethem, Priyanka Kumari, Bruno Boulanger, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
September 9, 2023
A multi-target QSRR approach to model retention times of small molecules in RPLC
Priyanka Kumari, Thomas Van Laethem, Diane Duroux, et al.
Molecules (Basel, Switzerland)
|
December 11, 2022
User-Driven Strategy for In Silico Screening of Reversed-Phase Liquid Chromatography Conditions for Known Pharmaceutical-Related Small Molecules
Thomas Van Laethem, Priyanka Kumari, Bruno Boulanger, et al.
Journal of Chromatography. A
|
April 11, 2007
Analysis of recent pharmaceutical regulatory documents on analytical method validation
Eric Rozet, Attilio Ceccato, Cédric Hubert, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|
June 25, 2018
Implementation of a generic SFC-MS method for the quality control of potentially counterfeited medicinal cannabis with synthetic cannabinoids
Hugues Jambo, Amandine Dispas, Hermane T Avohou, et al.
Page
of 2