Zobrazeno 1 - 10
of 134
pro vyhledávání: '"Christopher M. Riley"'
Publikováno v:
AAPS Open, Vol 2, Iss 1, Pp 1-9 (2016)
Abstract The computer program ASAPprime® has been used successfully for some time to predict the stability of active pharmaceutical ingredients (APIs) in solid-dosage forms. In this study, we have demonstrated that the ASAPprime® program can also b
Externí odkaz:
https://doaj.org/article/617ca5055f51475ca1679927e58f3a2b
Specification of Drug Substances and Products: Development and Validation of Analytical Methods is a comprehensive and critical analysis of the requirements and approaches to setting specifications for new pharmaceutical products, with an emphasis on
Autor:
Christopher M. Riley, Jessica M. L. Elwood, Martyn C. Henry, Irene Hunter, J. Daniel Lopez‐Fernandez, Iain J. McEwan, Craig Jamieson
Publikováno v:
Medicinal Research Reviews.
Autor:
Christopher M. Riley, K. Lien Nguyen
Specification of Drug Substances and Drug Products is a fully comprehensive reference on Specification Setting for Pharmaceuticals. There have been several recent developments in the ICH Guidelines, which were not captured in previous editions, notab
Publikováno v:
Occupational Hazards of Pesticide Exposure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d58fd9e673e30092c47a4f8232e015a
https://doi.org/10.1201/9781003075424-2
https://doi.org/10.1201/9781003075424-2
Autor:
Sean Letourneau, Trevor Williams, Dominic Godine, Eric Palmer, Jacob Hollister, Christopher M. Riley, Yohannes T. Tedla, Neil Ottenstein, Seth Shulman
Publikováno v:
2020 IEEE Aerospace Conference.
Launch window design for the Magnetospheric Multiscale (MMS) mission ensured that no excessive eclipses would be encountered during the prime mission. However, no orbit solutions exist that satisfy the eclipse constraints indefinitely: most extended
This chapter deals with the validation of assay and impurities methods for “small molecules.” The general principles described here are also generally applicable to “large molecules”; however, more than one test is usually necessary to charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::705879e90dfc2cb4a7769f0ce578b216
https://doi.org/10.1016/b978-0-08-102824-7.00011-7
https://doi.org/10.1016/b978-0-08-102824-7.00011-7
Autor:
Christopher M. Riley, A.M. Clarke
This chapter describes the rational design of analytical methods for assay and impurities designed to ensure adequate performance during the life cycle of the method for a given sample type. Method development starts with selection of the most approp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::091ca71942af27bd0a713f535900d880
https://doi.org/10.1016/b978-0-08-102824-7.00010-5
https://doi.org/10.1016/b978-0-08-102824-7.00010-5
Chapters 9, 10, and 11 present general concepts of assay and impurity analysis of drug substances and drug products. Discussion of current analytical methodologies for evaluation of impurities and assay and validation of method are presented in Chapt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c15f5e820055bf20c8e059f7372f0513
https://doi.org/10.1016/b978-0-08-102824-7.00009-9
https://doi.org/10.1016/b978-0-08-102824-7.00009-9