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

WHO Expert Committee on Biological Standardization fifty-sixth report.
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WHO Expert Committee on Specifications for Pharmaceutical Preparations thirty-seventh report.
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Good manufacturing practices for pharmaceuticals a plan for total quality control from manufacturer to consumer /
由: Willig, Sidney H., 1919-
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WHO Expert Committee on Specifications for Pharmaceutical Preparations fortieth report.
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WHO Expert Committee on Specifications for Pharmaceutical Preparations thirty-ninth report.
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WHO Expert Committee on Biological Standardization : sixty-third report. /
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The selection and use of essential medicines
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WHO Expert Committee on Biological Standardization fifty-second report.
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WHO Expert Committee on Biological Standardization fifty-fourth report.
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WHO Expert Committee on Biological Standardization : sixty-first report.
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Pharmaceutical drug analysis methodology - theory - instrumentation - pharmaceutical assays - cognote assays.
由: Kar, Ashutosh
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Reviews in pharmaceutical and biomedical analysis
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Biomedical chromatography
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Organelle-specific pharmaceutical nanotechnology
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Specification of drug substances and products : development and validation of analytical methods /
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Rift-lines within European regulatory framework for biosimilars when taking heterogeneity and variation during lifecycle of the reference biologic and the biosimilar into account /
由: Osmane, Malik
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Pharmaceutical industry innovation and developments /
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Dielectric analysis of pharmaceutical systems
由: Craig, Duncan Q. M.
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Flow injection analysis of pharmaceuticals automation in the laboratory /
由: Martínez Calatayud, José
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Characterization of impurities and degradants using mass spectrometry
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HPLC methods for recently approved pharmaceuticals
由: Lunn, George
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Continuous processing in pharmaceutical manufacturing /
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Leachables and extractables handbook safety evaluation, qualification, and best practices applied to inhalation drug products /
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Pharmaceutical blending and mixing /
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Regulating pharmaceuticals in Europe striving for efficiency, equity and quality /
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The selection and use of essential medicines report of the WHO Expert Committee, 2002.
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The war against counterfeit medicine my story /
由: Akunyili, Dora Nkem
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The selection and use of essential medicines report of the WHO Expert Committee, 2003 ; (including the 13th Model List of Essential Medicines).
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Pharmaceutical production facilities design and applications /
由: Cole, Graham, 1934-
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Thirty-sixth report
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Drug monitoring by HPLC recent developments /
由: Samanidou, Victoria
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Effective drug regulation a multicountry study /
由: Ratanawijitrasin, Sauwakon
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The greening of pharmaceutical engineering. practice, analysis, and methodology /
由: Islam, Rafiqul, 1959-
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Manufacturing of pharmaceutical proteins : from technology to economy /
由: Behme, Stefan
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Integrated pharmaceutics applied preformulation, product design, and regulatory science /
由: Al-Achi, Antoine, 1955-
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ADME-enabling technologies for drug design and development
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