Search Results - "Cenna, R."

ISO 9001:2015 standard implementation in clinical trial centers: An exploratory analysis of benefits and barriers in Italy by Franchina, V., Stabile, S., Cenna, R., Mannozzi, F., Federici, I., Testoni, S., Sinno, V., Cagnazzo, C.

“…In the last decade many clinical research centers in Italy have increasingly implemented and improved their quality standards and effectiveness of processes…”
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Pharmacovigilance in no Profit Clinical Trial: Duties and Responsibilities for the Research Team by Cagnazzo, C, Cenna, R, Stabile, S, Sinno, V, Testoni, S, Mannozzi, F, Federici, I, Franchina, V

“…Introduction: The pharmacovigilance (PV) activities in no profit clinical trials mainly concern the identification and collection of safety events, signal…”
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1856P Electronic informed consent: The need to redesign the consent process for the digital era by Cagnazzo, C., Nanni, O., Di Costanzo, A., Cenna, R., Marchetti, F., La Verde, N., Frazzetto, A.

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1778P Clinical research at the time of COVID-19: A passion or a real job? by Cagnazzo, C., Testoni, S., Cenna, R., Guarrera, A., Monti, M., Stabile, S., Federici, I., Taverniti, C., Pirondi, S., Ferrari, A., Fragioli, F.

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