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FDA's Critical Path: Status, Priorities & Models for Collaboration, 2007
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Implementation of good manufacturing practice regulations for positron emission tomography radiopharmaceuticals: challenges and opportunities perceived by imaging thought leaders
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An integrated framework to evaluate customer service delivery: a study of electronic systems at FDA's Los Angeles Import Operations Branch
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Examining the regulatory framework for drug compounding: industry views and experiences
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Incentivizing quality in the manufacture of pharmaceuticals: manufacturers' views on quality ratings
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Current practices in pharmaceutical container closure development
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Validation master plans: progress of implementation within the pharmaceutical industry
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Clinical trials driven by investigator-sponsors: GCP compliance with or without previous industry sponsorship
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Comparative analysis of scFv and non-scFv based chimeric antigen receptors (CARs) against B cell maturation antigen (BCMA)
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Risk management and recalls: a survey of medical device manufacturers
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Using cognitive task analysis for capturing expert instruction of food safety training for novice employees
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Reprocessing of single-use medical devices: a survey investigation comparing the views of three unheard stakeholders
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Regulating cosmeceuticals in the United States: a cosmetic industry view
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Redefining urban food systems to identify optimal rooftop community garden locations: a site suitability analysis in Seattle, Washington
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Airway fire: extensive literature review and practice recommendations
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Airway fire: extensive literature review and practice recommendations
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Characteristics of high impact internal evaluation offices
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Microsoft Word - Jessica Porter Thesis final
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A survey analysis of transparency in three Asian regulatory agencies responsible for medical products
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The effect of cone beam computed tomography (CBCT) imaging on orthodontic diagnosis and treatment planning
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Regulatory agreements for drug development collaborations: practices in the medical products industry
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