The Biotech Revolution: What's Next for Innovation?
Join Egnyte at the premier biotech event of the year, Fierce Biotech Summit, 2023, in Boston from October 16-18.
Modern Computing for Better Outcomes in Life Sciences
The 2023 Egnyte for Life Sciences Virtual Summit brought together 15 experts and leaders within the biotech space. Together, we explored the past, present, and future state of modern computing and the role it plays in driving better outcomes in the life science industry. This bog provides an overview of some of the most important session at the Summit.
How MOMA Therapeutics Transformed Their Data Collaborative Process with Egnyte
For emerging biotechs, effective collaboration is critical but can also be challenging. With outsourced R&D operations, global teams, and external partners like CROs, biotechs need to securely share data and enable file access across their ecosystem. This blog showcases how Egnyte customer, MOMA Therapeutics transformed their data collaborative process.
Setting Up a New eTMF Study in Egnyte
Egnyte’s eTMF allows you to assemble all the critical documentation related to your clinical trial so that you stay on track and are always audit-ready. Running your own eTMF gives you full visibility and control over data that is critical to the success of your company. In this article, you’ll learn how to set up a new study in Egnyte’s eTMF app.
How to Import your Historical Controlled Documents into Egnyte
If you’re a quality professional then you know that maintaining compliance, audit, and tracking of your controlled documents is critical. When you adopt Egnyte’s Controlled Document Management, you’ll have all of the tools to review, approve, release, and train your users on your policies, procedures, and other controlled docs. In this article, you’ll learn how to import your existing SOPs, work instructions, and other controlled documents into the Egnyte Controlled Document Management app.
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.