WHO Expert Committee on Biological Standardization : sixtieth report /

WHO Expert Committee on Biological Standardization fifty-fourth report.
Publié: (2005)

WHO Expert Committee on Biological Standardization fifty-second report.
Publié: (2004)

WHO Expert Committee on Specifications for Pharmaceutical Preparations forty-first report.
Publié: (2007)

WHO Expert Committee on Specification for Pharmaceutical Preparations forty-second report.
Publié: (2008)

The selection and use of essential medicines
Publié: (2006)

WHO Expert Committee on Specifications for Pharmaceutical Preparations : forty-eighth meeting report /
Publié: (2014)

WHO Expert Committee on Specifications for Pharmaceutical Preparations fortieth report.
Publié: (2006)

WHO Expert Committee on Specifications for Pharmaceutical Preparations thirty-ninth report.
Publié: (2005)

WHO Expert Committee on Specifications for Pharmaceutical Preparations thirty-seventh report.
Publié: (2003)

Good manufacturing practices for pharmaceuticals a plan for total quality control from manufacturer to consumer /
par: Willig, Sidney H., 1919-
Publié: (2000)

Rift-lines within European regulatory framework for biosimilars when taking heterogeneity and variation during lifecycle of the reference biologic and the biosimilar into account /
par: Osmane, Malik
Publié: (2014)

The selection and use of essential medicines report of the WHO Expert Committee, 2002.
Publié: (2003)

The selection and use of essential medicines report of the WHO Expert Committee, 2003 ; (including the 13th Model List of Essential Medicines).
Publié: (2004)

Pharmaceutical drug analysis methodology - theory - instrumentation - pharmaceutical assays - cognote assays.
par: Kar, Ashutosh
Publié: (2005)

Reviews in pharmaceutical and biomedical analysis
Publié: (2010)

Standardizing medication labels confusing patients less : workshop summary /
Publié: (2008)

Characterization of impurities and degradants using mass spectrometry
Publié: (2011)

The war against counterfeit medicine my story /
par: Akunyili, Dora Nkem
Publié: (2011)

Specification of drug substances and products : development and validation of analytical methods /
Publié: (2014)

Standardization studies from the Germanic languages /
Publié: (2002)

Dielectric analysis of pharmaceutical systems
par: Craig, Duncan Q. M.
Publié: (1995)

Flow injection analysis of pharmaceuticals automation in the laboratory /
par: Martínez Calatayud, José
Publié: (1996)

Development of FDA-regulated medical products : a translational approach /
par: Whitmore, Elaine
Publié: (2012)

HPLC methods for recently approved pharmaceuticals
par: Lunn, George
Publié: (2005)

Biomedical chromatography
Publié: (2010)

Drug monitoring by HPLC recent developments /
par: Samanidou, Victoria
Publié: (2010)

IFLA cataloguing principles steps towards an international cataloguing code, 3 : report from the 3rd IFLA Meeting of Experts on an International Cataloguing Code, Cairo, Egypt, 2005 /
Publié: (2006)

IFLA cataloguing principles steps towards an international cataloguing code, 4 : report from the 4th IFLA Meeting of Experts on an International Cataloguing Code, Seoul, Korea, 2006 /
Publié: (2007)

Thirty-sixth report
Publié: (2002)

Handbook of LC-MS bioanalysis best practices, experimental protocols, and regulations /
Publié: (2013)

Applications of ion chromatography for pharmaceutical and biological products
Publié: (2012)

Crisis standards of care summary of a workshop series /
Publié: (2010)

The development of science-based guidelines for laboratory animal care proceedings of the November 2003 international workshop /
Publié: (2004)

Analytical method validation and instrument performance verification
Publié: (2004)

Practical approaches to method validation and essential instrument performance verification
Publié: (2010)

Principios de catalogación IFLA hacia un código internacional de catalogación.
Publié: (2005)