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Tagged: eConsent

Impact of COVID 19 on the future of Rare Diseases and Oncology Clinical Trials

December 1st, 2020 | eConsent

FDA guidance (March 2020 and updated July 2020) acknowledged that the impact of COVID-19 may require companies conducting clinical trials to consider virtual patient visits or put new processes in place regarding their current protocols. Since COVID 19 has changed many of our normal way to conduct Clinical research, most organizations reported some level of […]

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