PharmaVigilant Enhances eTMF System Functionality
PharmaVigilant unveiled I-Vault 2.5, the enhanced version of its electronic Trial Master File (TMF) system. This new version offers easier access to trial data that sponsors use to make decisions related to their clinical trial. I-Vault 2.5 improves usability, administration and notification capabilities for site startup, site closeout and IRB submissions.
I-Vault 2.5 allows each sponsor to determine which trial documents they wish to collect and how they would like them organized.
“Sponsors need to convert their trial master files yesterday, so the need for robust, full-function products that can scale globally are in demand in the market. PharmaVigilant is committed to aggressive investments in our technology, and as a result we are widening the gap between ours and our competitors’ offerings,” said James DeSanti, founder and CEO of PharmaVigilant.
The newest version of I-Vault 2.5 includes key features such as:
· Enhanced e-mail notifications – allows trial sponsors to subscribe all users of a certain role to a notification.
· Enhanced document tracking capabilities – automatically send e-mails to designated users when an action has occurred on the select document they are tracking.
· Improved reporting functionality – users can view their documents in charts broken down by status, site or type, improving transparency and organization of files.
· Separated signed and approval status – provides increased visibility for users.
FDA Finalizes Decentralized Clinical Trial Guidance
November 25th 2024The FDA's guidance is part of a broader effort to modernize clinical trials, improve efficiency, reduce participant burden, and expand access, particularly for underrepresented populations and those in geographically or economically constrained areas.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
Patient Engagement Platform Checklist
November 22nd 2024Modern clinical trials are more complex than ever, and one significant reason is the increased focus on patient engagement. Incorporating a patient engagement platform into your clinical trial enhances the patient experience and can lead to more successful trials with stronger, more reliable outcomes. We put together this helpful checklist of key features to look out for when choosing a platform for your study.
The Rise of Predictive Engagement Tools in Clinical Trials
November 22nd 2024Patient attrition can be a significant barrier to the success of a randomized controlled trial (RCT). Today, with the help of AI-powered predictive engagement tools, clinical study managers are finding ways to proactively reduce attrition rates in RCTs, and increase the effectiveness of their trial. In this guide, we look at the role AI-powered patient engagement tools play in clinical research, from the problems they’re being used to solve to the areas and indications in which they’re being deployed.
