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

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

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

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

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

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

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

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

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

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

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

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

Reviews in pharmaceutical and biomedical analysis
Udgivet: (2010)

Biomedical chromatography
Udgivet: (2010)

Organelle-specific pharmaceutical nanotechnology
Udgivet: (2010)

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

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

Pharmaceutical industry innovation and developments /
Udgivet: (2011)

Dielectric analysis of pharmaceutical systems
af: Craig, Duncan Q. M.
Udgivet: (1995)

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

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

HPLC methods for recently approved pharmaceuticals
af: Lunn, George
Udgivet: (2005)

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

Continuous processing in pharmaceutical manufacturing /
Udgivet: (2015)

Pharmaceutical blending and mixing /
Udgivet: (2015)

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

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

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

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

Pharmaceutical production facilities design and applications /
af: Cole, Graham, 1934-
Udgivet: (1998)

Thirty-sixth report
Udgivet: (2002)

Drug monitoring by HPLC recent developments /
af: Samanidou, Victoria
Udgivet: (2010)

Effective drug regulation a multicountry study /
af: Ratanawijitrasin, Sauwakon
Udgivet: (2002)

Manufacturing of pharmaceutical proteins : from technology to economy /
af: Behme, Stefan
Udgivet: (2015)

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

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

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