‍ In clinical research, the process of uploading and managing lab data is rife with obstacles. Some of those obstacles threaten to derail productivity, which delays deployment and drives up costs – time is money, after all, and the longer the research phase takes, the more organizations are forced to spend on staffing and other resources. Here’s an overview of the major obstacles biotech organizations are facing today.

‍ As a contract research organization (CRO), your greatest responsibility is to be a reliable partner to the sponsor in executing a clinical trial. This can include tasks such as writing the study protocol, collecting and submitting data to the FDA, and monitoring sites throughout the study. To honor that responsibility, a CRO must have the right tools and skills to securely share trial data and collaborate with the sponsor.

‍ 2022 is coming to a close, and we’re excited to bring you one last round of improvements to the Egnyte platform just in time for the beginning of a new year. This month, we’ve got updates to watermarking for viewer-only permissions, UX improvements across the platform, AutoCAD DWG file preview for the Egnyte Android app, and various enhancements to our Migration App. Read all about it below.

‍ Without a doubt, data privacy will be a much bigger focus for small- and medium-sized businesses in 2023, as the U.S. states of California, Colorado, Connecticut, Utah, and Virginia all enact stricter privacy legislation. Similarly, the Canadian province of Quebec is also in the process of updating its data privacy laws.