NextDocs Announces Partnership with Thomson Reuters
Philadelphia, PA- September 17, 2009
NextDocs Corporation announced enhancements to their partnership with Thomson Reuters, a leading source of intelligent information for businesses and professionals. Together, the companies have developed and demonstrated effective integration between the NextDocs Document and Quality Management System and the Thomson Reuters Liquent Regulatory software platform, providing a comprehensive solution for managing regulatory content from authoring to publishing and submission. In addition, the two companies also announced that NextDocs will support the Liquent SmartScribe® set of document templates from Thomson Reuters.
The integration between the NextDocs Document and Quality Management System and the Liquent InSight Platform allows the two systems to work from a common set of SharePoint-based documents. With SharePoint as a common repository, NextDocs system and theLiquent Regulatory Software are able to interact with one another; for example, organizations can access NextDocs documents housed in SharePoint and build an eCTD structure utilizing Thomson Reuters Liquent InSight Platform.
"Our Liquent InSight platform...provide[s] a single authoritative platform, which allows users to manage regulatory information through all stages of development, from early submissions to marketed registrations," said Rick Riegel, Vice President and General Manager, Services and Software Solutions at Thomson Reuters.
As part of the enhanced partnership, NextDocs will be offering Liquent SmartScribe® from Thomson Reuters. These templates enable users to create common technical documents quickly, efficiently and in a constant standard. The user friendly templates help to ensure all documents comply with format requirements.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
Reaching Diverse Patient Populations With Personalized Treatment Methods
January 20th 2025Daejin Abidoye, head of solid tumors, oncology development, AbbVie, discusses a number of topics around diversity in clinical research including industry’s greatest challenges in reaching diverse patient populations, personalized treatment methods, recruitment strategies, and more.
