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

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

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

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

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

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

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

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

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

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

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

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

Reviews in pharmaceutical and biomedical analysis
Publicado: (2010)

Biomedical chromatography
Publicado: (2010)

Organelle-specific pharmaceutical nanotechnology
Publicado: (2010)

Specification of drug substances and products : development and validation of analytical methods /
Publicado: (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 /
por: Osmane, Malik
Publicado: (2014)

Pharmaceutical industry innovation and developments /
Publicado: (2011)

Dielectric analysis of pharmaceutical systems
por: Craig, Duncan Q. M.
Publicado: (1995)

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

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

HPLC methods for recently approved pharmaceuticals
por: Lunn, George
Publicado: (2005)

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

Continuous processing in pharmaceutical manufacturing /
Publicado: (2015)

Pharmaceutical blending and mixing /
Publicado: (2015)

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

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

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

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

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

Thirty-sixth report
Publicado: (2002)

Drug monitoring by HPLC recent developments /
por: Samanidou, Victoria
Publicado: (2010)

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

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

Effective drug regulation a multicountry study /
por: Ratanawijitrasin, Sauwakon
Publicado: (2002)

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

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