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Nina S Cauchon

Showing results (1-10 of 13) with videos related to

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Journal of Pharmaceutical Sciences|February 1, 2020
Transitioning Chemistry, Manufacturing, and Controls Content With a Structured Data Management Solution: Streamlining Regulatory SubmissionsMarquerita Algorri, Nina S Cauchon, Michael J Abernathy
Journal of Pharmaceutical Sciences|February 23, 2019
Innovation in Chemistry, Manufacturing, and Controls-A Regulatory Perspective From IndustryNina S Cauchon, Shirley Oghamian, Soraya Hassanpour, et al.
Journal of Pharmaceutical and Biomedical Analysis|April 7, 2007
Identification of volatile degradants in formulations containing sesame oil using SPME/GC/MSWencan Chen, Pengzu Zhou, Kirby C Wong-Moon, et al.
Journal of Pharmaceutical Sciences|February 5, 2023
Patient-Centric Product Development: A Summary of Select Regulatory CMC and Device ConsiderationsMarquerita Algorri, Nina S Cauchon, Twinkle Christian, et al.
Journal of Pharmaceutical Sciences|September 24, 2020
The Confluence of Innovation in Therapeutics and Regulation: Recent CMC ConsiderationsLucas Gutierrez, Nina S Cauchon, Twinkle R Christian, et al.
Journal of Pharmaceutical Sciences|February 6, 2026
Pioneering the future: Delivering the first digitally generated CMC post-approval change (PAC) dossier to global regulators simultaneouslyMarquerita Algorri, Nina S Cauchon, Kabir Ahluwalia, et al.
Journal of Pharmaceutical Sciences|September 3, 2021
Re-Envisioning Pharmaceutical Manufacturing: Increasing Agility for Global Patient AccessMarquerita Algorri, Michael J Abernathy, Nina S Cauchon, et al.
AAPS Open|May 16, 2023
Structured content and data management-enhancing acceleration in drug development through efficiency in data exchangeJill Beierle, Marquerita Algorri, Marisol Cortés, et al.
Molecular Pharmaceutics|August 13, 2010
Development and application of a biorelevant dissolution method using USP apparatus 4 in early phase formulation developmentJiang B Fang, Vivian K Robertson, Archana Rawat, et al.
Journal of Pharmaceutical Sciences|December 26, 2024
Advancing the implementation of innovative analytical technologies in pharmaceutical manufacturing-Some regulatory considerationsTing Wang, Nina S Cauchon, J Paul Kirwan, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Journal of Pharmaceutical Sciences|February 1, 2020
Transitioning Chemistry, Manufacturing, and Controls Content With a Structured Data Management Solution: Streamlining Regulatory SubmissionsMarquerita Algorri, Nina S Cauchon, Michael J Abernathy
Journal of Pharmaceutical Sciences|February 23, 2019
Innovation in Chemistry, Manufacturing, and Controls-A Regulatory Perspective From IndustryNina S Cauchon, Shirley Oghamian, Soraya Hassanpour, et al.
Journal of Pharmaceutical and Biomedical Analysis|April 7, 2007
Identification of volatile degradants in formulations containing sesame oil using SPME/GC/MSWencan Chen, Pengzu Zhou, Kirby C Wong-Moon, et al.
Journal of Pharmaceutical Sciences|February 5, 2023
Patient-Centric Product Development: A Summary of Select Regulatory CMC and Device ConsiderationsMarquerita Algorri, Nina S Cauchon, Twinkle Christian, et al.
Journal of Pharmaceutical Sciences|September 24, 2020
The Confluence of Innovation in Therapeutics and Regulation: Recent CMC ConsiderationsLucas Gutierrez, Nina S Cauchon, Twinkle R Christian, et al.
Journal of Pharmaceutical Sciences|February 6, 2026
Pioneering the future: Delivering the first digitally generated CMC post-approval change (PAC) dossier to global regulators simultaneouslyMarquerita Algorri, Nina S Cauchon, Kabir Ahluwalia, et al.
Journal of Pharmaceutical Sciences|September 3, 2021
Re-Envisioning Pharmaceutical Manufacturing: Increasing Agility for Global Patient AccessMarquerita Algorri, Michael J Abernathy, Nina S Cauchon, et al.
AAPS Open|May 16, 2023
Structured content and data management-enhancing acceleration in drug development through efficiency in data exchangeJill Beierle, Marquerita Algorri, Marisol Cortés, et al.
Molecular Pharmaceutics|August 13, 2010
Development and application of a biorelevant dissolution method using USP apparatus 4 in early phase formulation developmentJiang B Fang, Vivian K Robertson, Archana Rawat, et al.
Journal of Pharmaceutical Sciences|December 26, 2024
Advancing the implementation of innovative analytical technologies in pharmaceutical manufacturing-Some regulatory considerationsTing Wang, Nina S Cauchon, J Paul Kirwan, et al.
Pageof 2