IntraLinks announced IntraLinks for Study Management, a secure, online platform for managing and monitoring all communication and activity with investigative sites and other outside parties during clinical trials from study start-up through study close-out. The new offering expands the full suite of IntraLinks’ solutions for clinical operations, which accelerates business processes, cuts costs, and reduces risks throughout the clinical trial lifecycle.
IntraLinks for Study Management specifically helps to:
· Centralize all study-related documents, communication and activity history in an organized, consistent, and searchable fashion
· Standardize and automate processes such as contract & budget negotiation, regulatory document distribution and collection and ongoing document exchange
· Eliminate repetitive and redundant site data entry and document submission
· Provide sites with a personalized view of tasks, requests and due dates, with reminder alerts and a secure communication channel to ensure timely site activation
· Monitor process progress with real-time activity dashboards and meet regulatory compliance with detailed access reports and audit trails
IntraLinks also offers a collaborative platform for site recruitment and safety reporting as part of its suite of solutions. IntraLinks for Site Recruitment enables users to eliminate the redundancy and manual tasks related to feasibility survey creation, distribution and collection. IntraLinks for Safety Document Exchange provides a secure environment where safety teams can receive notifications, route them for review, and instantaneously distribute subsequent letters to all parties requiring notification in an intelligent, automated, and auditable fashion.
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.
Zenocutuzumab Shows Durable Efficacy in NRG1 Fusion-Positive Cancers in Phase II eNRGy Trial
February 13th 2025The Phase II eNRGy trial showed durable antitumor activity with zenocutuzumab (Bizengri) in patients with NRG1 fusion–positive cancers, particularly non-small cell lung cancer and pancreatic cancer.
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.