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.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
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