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The urgency and impact of the ongoing COVID-19 pandemic are changing global drug development and regulatory processes. The need for speed to understand the virus and develop new vaccines, medicines, and therapies for patients has provided unprecedented learning opportunities and revealed how the pharmaceutical industry can improve upon traditional processes. To stay competitive while remaining compliant with agency regulations and guidance, companies need to implement new process/tools that allow for more flexible work models, consider expanding the use of decentralized/hybrid trials, and capitalize on the use of real-world evidence (RWE) and cloud-based data systems. In addition, regulatory agencies should retain the agility exhibited during current reviews of potential new therapies, applying this momentum to other areas of unmet medical need. Further, agencies should consider a globally acceptable application platform. This article, by the Pharmaceuticals’ Head of Regulatory Affairs at Bayer AG, examines how impacts of the COVID-19 crisis will continue beyond the pandemic period to the benefit of patients, drug developers, regulators, clinicians, and caregivers.
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10.1007/s43441-020-00239-8
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document_parses/pdf_json/266e325a566a09e063267ce8ad9e1e19448bfb01.json
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document_parses/pmc_json/PMC7687208.xml.json
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New Approaches to Regulatory Innovation Emerging During the Crucible of COVID-19: In Responding to a Global Health Crisis, Industry is Discovering New, Efficient Ways of Meeting Objectives
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