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Dissertation 4.3

Clinical Trials for Pharmaceutical Firms: Policy And Regulation | Post-Pandemic Lessons

10
Pages
APA
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~ 10–15 mins
Reading Time
Supply Chain Climate InsurTech
Abstract

This dissertation investigates “Clinical Trials for Pharmaceutical Firms: Policy And Regulation | Post-Pandemic Lessons” using a event study methodology. Through a institutional lens, the analysis integrates multi-source data to derive a stakeholder-aligned blueprint for researchers and practitioners.

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Clinical Trials for Pharmaceutical Firms: Policy And Regulation | Post-Pandemic Lessons

ABSTRACT
Clinical Trials for Pharmaceutical Firms: Policy And Regulation | Post-Pandemic Lessons is unpacked across themes: ethics, usability, security, and scalability. Limitations and future research paths are noted.
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