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Regulatory dissonance in the global development of drug therapies: a case study of drug development in postmenopausal osteoporosis
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Regulatory agreements for drug development collaborations: practices in the medical products industry
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Regulatory harmonization in a resource-limited setting: the World Health Organization Collaborative Procedure for Accelerated Registration
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“Regulatory” due diligence: a survey investigation of best practices in the medical products industry
A survey analysis of transparency in three Asian regulatory agencies responsible for medical products
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Regulatory team development in post-merger integration: a survey of views from medical product companies
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Examining the regulatory framework for drug compounding: industry views and experiences
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Estradiol regulation of cerebral metabolism: implications for neuroprotection and mitochondrial bioenergetics
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Convergence of United States regulatory and reimbursement policies impacting patient access to humanitarian use devices (HUD)
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Organizational communication of regulatory intelligence: a survey of the medical device industry
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Examining the cord blood industry views on the biologic license application regulatory framework
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Current practices in pharmaceutical container closure development
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Regulating cosmeceuticals in the United States: a cosmetic industry view
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Implementation of risk management in medical device companies: a survey analysis of current practices
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The impact of incomplete monographs on the OTC drug industry:  a survey investigation of industry views
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Validation master plans: progress of implementation within the pharmaceutical industry
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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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Risk management and recalls: a survey of medical device manufacturers
Current practices of U.S. investigators in the management of the clinical trial agreement: a survey of knowledge, attitudes, perceptions, and engagement
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An industry survey of implementation strategies for clinical supply chain management of cell and gene therapies
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Promotion of regulated products using social media: an industry view
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Challenges to implementation of alternative methods to animal testing for drug safety assessment in North America
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Benefits-risk frameworks: implementation by industry
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A survey of US industry views on implementation of decentralized clinical trials
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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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