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Practical approaches to operationalizing decentralized clinical trials
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Regulators Show Growing Interest In RWE For New Expanded Drug Indications
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PRA expands COVID-19 pharmacovigilance resources The CRO is offering an expanded range of post-authorization solutions designed to help developers with treatments and vaccines in their product pipeline
PRA Health Sciences has expanded its pharmacovigilance solutions to include a broader range of post-marketing services geared toward authorized vaccines and therapeutics for COVID-19. The offerings are designed to enable drug developers to keep up with the speed, accuracy and transparency demands of pharmacovigilance and safety data monitoring associated with COVID-19 treatments and vaccines.
Sabine Richter, vice president of pharmacovigilance and patient safety with PRA, said, “As more COVID-19 vaccines and therapeutics are approved, marketing authorization holders will have massive volumes of safety data to review and report in almost real-time. Our pharmacovigilance solutions enable clients to adhere to regulatory reporting and compliance standards a
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