Univo IRB provides a centralized, patient‑centric IRB service for Phase I‑IV clinical research, using its OneVerse® cloud platform to aggregate submissions, automate data entry, and track review status in real time. The solution offers role‑based dashboards, live chat, and a searchable knowledge base to streamline compliance and accelerate study start‑up for pharma, biotech, device sponsors, CROs, and academic groups.
Funding
Funding not disclosed
Founders
Product
Problem
Clinical trial sponsors face lengthy, fragmented IRB review processes that are bureaucratic, inconsistent, and often lack patient‑focused considerations, causing delays in study start‑up and increased administrative burden.
Solution
Univo IRB offers a single, patient‑centric IRB service that consolidates ethical review for Phase I‑IV pharmaceutical, device, biologic, behavioral, and psychosocial research. Its proprietary OneVerse® platform centralizes all submissions, auto‑populates repetitive data, and provides real‑time status tracking and messaging, reducing manual effort and errors. The system includes granular role‑based views, live chat support, and searchable resources to keep investigators informed and engaged. By emphasizing patient participation, education, and advocacy, Univo IRB streamlines compliance while safeguarding participant welfare, enabling faster regulatory approvals and study initiation.
Target Audience
Primary customers are pharmaceutical, biotech, and medical‑device sponsors, as well as CROs and academic research groups conducting clinical trials that require centralized IRB oversight.
Features
- OneVerse® cloud platform that aggregates all IRB submissions, amendments, and approvals in a single dashboard
- Dynamic form generation and auto‑population of recurring information to eliminate duplicate data entry
- Role‑based access controls delivering customized views for investigators, coordinators, and reviewers
- Integrated live chat and notification system for instant communication with the IRB team
- Built‑in searchable knowledge base and resource library covering regulatory guidance and patient‑advocacy materials
- Reviewer tools that provide history, guidance, and analytics to accelerate decision‑making
- Secure, audit‑ready documentation storage with version control for all study documents