Abstract:Clinical drug development is a complex and extensive process that entails multiple stakeholders alongside patients, requires large capital expenditures and takes nearly a decade on average to complete. To ensure the correct development of this process, rigorous quality activities must be conducted to assess and guarantee the Good Clinical and Pharmacovigilance Practices (GxP) for study compliance. For about 25 years, most of these activities have been performed in the form of audits, which implies a high volum… Show more
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