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WHO Expert Committee on Biological Standardization : sixtieth report /
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WHO Expert Committee on Biological Standardization fifty-sixth report.
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WHO Expert Committee on Specifications for Pharmaceutical Preparations : forty-eighth meeting report /
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Good manufacturing practices for pharmaceuticals a plan for total quality control from manufacturer to consumer /
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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 : sixty-first report.
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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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Pharmaceutical drug analysis methodology - theory - instrumentation - pharmaceutical assays - cognote assays.
द्वारा: Kar, Ashutosh
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Reviews in pharmaceutical and biomedical analysis
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Specification of drug substances and products : development and validation of analytical methods /
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Dielectric analysis of pharmaceutical systems
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The selection and use of essential medicines report of the WHO Expert Committee, 2002.
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Flow injection analysis of pharmaceuticals automation in the laboratory /
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Tests and general requirements for dosage forms ; quality specifications for pharmaceutical substances and tablets
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HPLC methods for recently approved pharmaceuticals
द्वारा: Lunn, George
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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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Characterization of impurities and degradants using mass spectrometry
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Continuous processing in pharmaceutical manufacturing /
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Neonatal formulary 5 drug use in pregnancy and the first year of life /
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Biomedical chromatography
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Drug monitoring by HPLC recent developments /
द्वारा: Samanidou, Victoria
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WHO Expert Committee on Drug Dependence thirty-fourth report.
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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 /
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WHO Expert Committee on Drug Dependence thirty-third report.
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Neonatal formulary 7 : drug use in pregnancy and the first year of life.
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Handbook of LC-MS bioanalysis best practices, experimental protocols, and regulations /
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Understanding the benefits and risks of pharmaceuticals workshop summary, Forum on Drug Discovery, Development, and Translation, Board on Health Sciences Policy /
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Quality assurance of pharmaceuticals a compendium of guidelines and related materials. Volume 2, Good manufacturing practices and inspection.
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Evaluation of certain veterinary drug residues in food sixty-sixth report of the Joint FAO/WHO Expert Committee on Food Additives.
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Extractables & Leachables for Pharmaceutical Products 2011 : [conference proceedings] : Dublin, Ireland, 27-28 September 2011 /
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Practical approaches to method validation and essential instrument performance verification
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Analytical method validation and instrument performance verification
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