As life sciences companies grow, the regulatory compliance requirements and risks expand as well. These responsibilities extend beyond conventional health-related frameworks (e.g. GxP, HIPAA, etc.) into the realm of data privacy. For high-growth institutions with limited resources & bandwidth, the question arises: what should you do? In this document, Egnyte chronicles some of the regulations affecting the life sciences industry and share 5 activities to help your organization comply with these new and dynamic laws.
EHR-to-EDC Technology: A Guide to Modern Data Acquisition in Oncology Clinical Trials
December 20th 2023Inside this eBook, readers can expect to learn how to effectively navigate the various challenges associated with clinical trial data collection and reporting in the age of digitalization and at a time in which site staff are experiencing turnover and seeking more efficiency.