PharmaVigilant introduced the latest version of its leading electronic Trial Master File system, I-Vault 2.6. The new enhancements addresses sponsors needs in customized workflow, bulk imports and improved reporting.
“Since its inception, I-Vault eTMF was designed to collect, manage, and organize all documents relating to a sponsors clinical trial or program.” I-Vault 2.6 now offers barcode recognition technology that will read barcode(s) from scanned files. By adding barcodes to our system generated Source Worksheets for example, users have the ability to do bulk or batch scans into I-Vault, which reads the file’s barcode and determines where the document should be placed within the system. This feature enhances our remote Source Document Verification service, streamlining the scanning process so documents are available in their correct placeholders sooner for EDC comparison.
With new OCR capability, I-Vault can now capture the contents of a scanned document and store it within the system. This allows users to convert their paper documents into searchable PDFs for text search purposes. This functionality also enables you to quickly locate content within the system based on a keyword search.
The enhancement to system notifications creates a more user based system with alerts and views of data catered to the authenticated user. When a notification is now created, it can be specified whether it should be sent to the user responsible for reviewing the document via email. This in turn eases the ability to monitor the TMF content across the life of the study.
I-Vault 2.6 also configures document dependencies to streamline the workflow. The Sponsor can now set the system to require a certain document or folder upon the upload or modified status of another document. Additionally, it can be specified whether certain document types require translations.
The digital signature feature of the system has been updated to allow I-Vault users to reach wholly electronic workflows through the authorization stage: Signatures are now embedded into the PDF so that information will never become disconnected from the document itself. This ensures that end users can easily verify and retain proof of identity and document integrity without costly, complicated, or proprietary software. The ability to add multiple signatures to a document is also supported.
The Importance of Real-World Evidence in Medical Research and Drug Development
February 18th 2025The ongoing evolution of real-world evidence from a novel concept to a cornerstone of modern medical research signifies its growing importance and vast potential to improve personalized medicine, overall healthcare outcomes, and eventually democratization of scientific facts by general accessibility.
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.
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.