Note: This sponsored techXpo session does not provide ACRP Contact Hours. By participating, you consent to ACRP sharing your name, title, organization, and physical mailing address with the techXpo session sponsor.
Kate Yawman, Director of Product Management, Advarra
More than ever before, clinical research professionals are increasingly looking for ways to modernize their operations, recognizing that the changes of the past year have accelerated the acceptance and availability of technology that can deliver streamlined regulatory processes. These solutions have enabled capabilities related to decentralized or hybrid trials and can create a more patient-centric experience. However, regulatory compliance is still paramount, and this session will cover how sites can not only maintain but enhance compliance while evolving their research programs to keep pace with the changing research landscape. Join Advarra to learn how implementing eRegulatory & eConsent systems can improve compliance and productivity, and reduce cost; Understand how to assess what regulatory requirements apply to remote work enabling software for clinical research, and identify opportunities for research programs to advance the way they do research in a changing environment.
This techXpo session is sponsored by Advarra, in conjunction with ACRP 2021.
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