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Perspective on Quality Risk Management of Pharmaceutical Quality
Drug Information Journal, 2007Quality risk management for the pharmaceutical industry was recently defined in internationally harmonized guidance as a systematic process for the assessment, control, communication, and review of risks to the quality of the drug product across the product life cycle.
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Specification vagueness and supply quality risk
Naval Research Logistics (NRL), 2013AbstractSpecifying quality requirement is integral to any sourcing relationship, but vague and ambiguous specifications can often be observed in practice, especially when a buyer is in the initial stage of sourcing a new product. In this research, we study a supplier's production incentives under vague or exact quality specifications.
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Corporate carbon risk exposure, voluntary disclosure, and financial reporting quality
Business Strategy and the Environment, 2020Tesfaye T Lemma +2 more
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Quality versus Risk-of-Bias assessment in clinical research
Journal of Clinical Epidemiology, 2021Luis Furuya-Kanamori +2 more
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