Automating Instrument Data Ingestion and Access to Accelerate Lab Productivity
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, as the longer the research phase takes, the more organizations are forced to spend on staffing and other resources. This blog post gives an overview of the major obstacles biotech organizations are facing today when managing lab data.
How Egnyte Enables Secure File Sharing and Collaboration for CROs
The greatest responsibility of a contract research organization (CRO) 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. This article will explore what is at stake when it comes to CRO-to-sponsor data sharing and collaboration, and how CROs can leverage Egnyte to give study sponsors confidence that trial data is secure, compliant, and properly governed.
Top Considerations for Building a Lab-to-Cloud Workflow
Enormous volumes of clinical data generated in life sciences lab settings need to be shared globally to cloud-based repositories, and made accessible to myriad remote stakeholders. Any organization hoping to extract immediate value from this data is tasked with building a lab-to-cloud data workflow that is scalable, has integrity, and allows for granular control and oversight. This post explores the top technology considerations in building a lab-to-cloud workflow.