WHO Expert Committee on Specification for Pharmaceutical Preparations forty-second report.

WHO Expert Committee on Biological Standardization fifty-sixth report.
Gepubliceerd in: (2007)

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

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

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

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

WHO Expert Committee on Biological Standardization : sixty-third report. /
Gepubliceerd in: (2014)

The selection and use of essential medicines
Gepubliceerd in: (2006)

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

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

WHO Expert Committee on Biological Standardization : sixty-first report.
Gepubliceerd in: (2013)

Pharmaceutical drug analysis methodology - theory - instrumentation - pharmaceutical assays - cognote assays.
door: Kar, Ashutosh
Gepubliceerd in: (2005)

Reviews in pharmaceutical and biomedical analysis
Gepubliceerd in: (2010)

Biomedical chromatography
Gepubliceerd in: (2010)

Organelle-specific pharmaceutical nanotechnology
Gepubliceerd in: (2010)

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

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

Pharmaceutical industry innovation and developments /
Gepubliceerd in: (2011)

Dielectric analysis of pharmaceutical systems
door: Craig, Duncan Q. M.
Gepubliceerd in: (1995)

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

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

HPLC methods for recently approved pharmaceuticals
door: Lunn, George
Gepubliceerd in: (2005)

Leachables and extractables handbook safety evaluation, qualification, and best practices applied to inhalation drug products /
Gepubliceerd in: (2012)

Continuous processing in pharmaceutical manufacturing /
Gepubliceerd in: (2015)

Pharmaceutical blending and mixing /
Gepubliceerd in: (2015)

Regulating pharmaceuticals in Europe striving for efficiency, equity and quality /
Gepubliceerd in: (2004)

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

The war against counterfeit medicine my story /
door: Akunyili, Dora Nkem
Gepubliceerd in: (2011)

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

Pharmaceutical production facilities design and applications /
door: Cole, Graham, 1934-
Gepubliceerd in: (1998)

Thirty-sixth report
Gepubliceerd in: (2002)

Drug monitoring by HPLC recent developments /
door: Samanidou, Victoria
Gepubliceerd in: (2010)

Manufacturing of pharmaceutical proteins : from technology to economy /
door: Behme, Stefan
Gepubliceerd in: (2015)

The greening of pharmaceutical engineering. practice, analysis, and methodology /
door: Islam, Rafiqul, 1959-
Gepubliceerd in: (2015)

Integrated pharmaceutics applied preformulation, product design, and regulatory science /
door: Al-Achi, Antoine, 1955-
Gepubliceerd in: (2013)

Effective drug regulation a multicountry study /
door: Ratanawijitrasin, Sauwakon
Gepubliceerd in: (2002)

ADME-enabling technologies for drug design and development
Gepubliceerd in: (2012)