Pharmaceutical drug analysis methodology - theory - instrumentation - pharmaceutical assays - cognote assays.
Сохранить в:
| Главный автор: | |
|---|---|
| Соавтор: | |
| Формат: | Электронный ресурс eКнига |
| Язык: | английский |
| Опубликовано: |
New Delhi :
New Age International (P) Ltd., Publishers,
2005.
|
| Редактирование: | 2nd ed. |
| Предметы: | |
| Online-ссылка: | An electronic book accessible through the World Wide Web; click to view |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|
Схожие документы
Reviews in pharmaceutical and biomedical analysis
Опубликовано: (2010)
Опубликовано: (2010)
Flow injection analysis of pharmaceuticals automation in the laboratory /
по: Martínez Calatayud, José
Опубликовано: (1996)
по: Martínez Calatayud, José
Опубликовано: (1996)
Dielectric analysis of pharmaceutical systems
по: Craig, Duncan Q. M.
Опубликовано: (1995)
по: Craig, Duncan Q. M.
Опубликовано: (1995)
HPLC methods for recently approved pharmaceuticals
по: Lunn, George
Опубликовано: (2005)
по: Lunn, George
Опубликовано: (2005)
Specification of drug substances and products : development and validation of analytical methods /
Опубликовано: (2014)
Опубликовано: (2014)
WHO Expert Committee on Specification for Pharmaceutical Preparations forty-second report.
Опубликовано: (2008)
Опубликовано: (2008)
WHO Expert Committee on Specifications for Pharmaceutical Preparations forty-first report.
Опубликовано: (2007)
Опубликовано: (2007)
Drug monitoring by HPLC recent developments /
по: Samanidou, Victoria
Опубликовано: (2010)
по: Samanidou, Victoria
Опубликовано: (2010)
Characterization of impurities and degradants using mass spectrometry
Опубликовано: (2011)
Опубликовано: (2011)
Biomedical chromatography
Опубликовано: (2010)
Опубликовано: (2010)
Good manufacturing practices for pharmaceuticals a plan for total quality control from manufacturer to consumer /
по: Willig, Sidney H., 1919-
Опубликовано: (2000)
по: Willig, Sidney H., 1919-
Опубликовано: (2000)
Analytical method validation and instrument performance verification
Опубликовано: (2004)
Опубликовано: (2004)
Practical approaches to method validation and essential instrument performance verification
Опубликовано: (2010)
Опубликовано: (2010)
Handbook of LC-MS bioanalysis best practices, experimental protocols, and regulations /
Опубликовано: (2013)
Опубликовано: (2013)
The selection and use of essential medicines
Опубликовано: (2006)
Опубликовано: (2006)
Drug-drug interactions in pharmaceutical development
Опубликовано: (2008)
Опубликовано: (2008)
WHO Expert Committee on Biological Standardization fifty-sixth report.
Опубликовано: (2007)
Опубликовано: (2007)
WHO Expert Committee on Biological Standardization : sixtieth report /
Опубликовано: (2013)
Опубликовано: (2013)
Who Expert Committee on Biological Standardization : sixty-second report.
Опубликовано: (2013)
Опубликовано: (2013)
Pharmaceutical toxicology in practice a guide for non-clinical development /
Опубликовано: (2011)
Опубликовано: (2011)
Rift-lines within European regulatory framework for biosimilars when taking heterogeneity and variation during lifecycle of the reference biologic and the biosimilar into account /
по: Osmane, Malik
Опубликовано: (2014)
по: Osmane, Malik
Опубликовано: (2014)
The greening of pharmaceutical engineering. practice, analysis, and methodology /
по: Islam, Rafiqul, 1959-
Опубликовано: (2015)
по: Islam, Rafiqul, 1959-
Опубликовано: (2015)
Statistical thinking for non-statisticians in drug regulation /
по: Kay, R. (Richard), 1949-
Опубликовано: (2015)
по: Kay, R. (Richard), 1949-
Опубликовано: (2015)
Analysis of aggregates and particles in protein pharmaceuticals
Опубликовано: (2012)
Опубликовано: (2012)
Physiological pharmaceutics barriers to drug absorption /
по: Washington, Neena, 1961-
Опубликовано: (2001)
по: Washington, Neena, 1961-
Опубликовано: (2001)
Drug discovery and design medical aspects /
Опубликовано: (2002)
Опубликовано: (2002)
Target validation in drug discovery
Опубликовано: (2006)
Опубликовано: (2006)
Drugs and laboratory parameters
по: Caputi, Achille Patrizio
Опубликовано: (2010)
по: Caputi, Achille Patrizio
Опубликовано: (2010)
The war against counterfeit medicine my story /
по: Akunyili, Dora Nkem
Опубликовано: (2011)
по: Akunyili, Dora Nkem
Опубликовано: (2011)
Human drug targets : a compendium for pharmaceutical discovery /
по: Zanders, Edward D.
Опубликовано: (2016)
по: Zanders, Edward D.
Опубликовано: (2016)
Computational pharmaceutics : application of molecular modeling in drug delivery /
Опубликовано: (2015)
Опубликовано: (2015)
Continuous processing in pharmaceutical manufacturing /
Опубликовано: (2015)
Опубликовано: (2015)
Mass spectrometry in sports drug testing characterization of prohibited substances and doping control analytical assays /
по: Thevis, Mario, 1973-
Опубликовано: (2010)
по: Thevis, Mario, 1973-
Опубликовано: (2010)
Pharmaceutical applications of polymers for drug delivery
по: Jones, David
Опубликовано: (2004)
по: Jones, David
Опубликовано: (2004)
Pharmaceutical industry innovation and developments /
Опубликовано: (2011)
Опубликовано: (2011)
Predictive approaches in drug discovery and development biomarkers and in vitro/in vivo correlations /
Опубликовано: (2012)
Опубликовано: (2012)
Pharmaceuticals
Опубликовано: (2012)
Опубликовано: (2012)
Successfully marketing clinical trial results winning in the healthcare business /
по: Umbach, Günter
Опубликовано: (2006)
по: Umbach, Günter
Опубликовано: (2006)
Evaluation of drug candidates for preclinical development pharmacokinetics, metabolism, pharmaceutics, and toxicology /
Опубликовано: (2010)
Опубликовано: (2010)
Integrated cardiac safety assessment methodologies for noncardiac drugs in discovery, development, and postmarketing surveillance /
по: Turner, J. Rick
Опубликовано: (2009)
по: Turner, J. Rick
Опубликовано: (2009)