WHO Expert Committee on Biological Standardization : sixtieth report /

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

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

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

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

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

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

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

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

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

Good manufacturing practices for pharmaceuticals a plan for total quality control from manufacturer to consumer /
Autor: Willig, Sidney H., 1919-
Vydáno: (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 /
Autor: Osmane, Malik
Vydáno: (2014)

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

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

Reviews in pharmaceutical and biomedical analysis
Vydáno: (2010)

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

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

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

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

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

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

Dielectric analysis of pharmaceutical systems
Autor: Craig, Duncan Q. M.
Vydáno: (1995)

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

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

HPLC methods for recently approved pharmaceuticals
Autor: Lunn, George
Vydáno: (2005)

Biomedical chromatography
Vydáno: (2010)

Drug monitoring by HPLC recent developments /
Autor: Samanidou, Victoria
Vydáno: (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 /
Vydáno: (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 /
Vydáno: (2007)

Thirty-sixth report
Vydáno: (2002)

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

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

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

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

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

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

Standards recipes for reality /
Autor: Busch, Lawrence
Vydáno: (2011)