Partner with Univo IRB for the participant-centered service and forward-thinking technology you need to navigate a changing industry and get independent IRB approval, faster.
The Univo IRB Difference
Exceptional Service
Customer service is woven into our IRB protocols. We go above other IRB companies in our collaboration, increasing visibility and decreasing ambiguity to ensure participant safety and compliance every step of the way.
Because our goal is to protect your patients, not try your patience.
- Weekly meetings
- Ad-hoc emergency meetings
- Daily expedited IRB review process
- Delivery of IRB documents 1-2 days after review
- Board decision notification within 24 hours of board meeting
- Competitive pricing
Most IRB companies average 90% of their time allocated to managing submissions and 10% for supporting clients.
At Univo IRB, our ratio is 60:40% because we know you need reliable access to IRB expertise.
Single Point of Contact
Unlike at other IRB committees where tired technology and workflows require multiple handoffs and cause delays, Univo IRB provides you with one account associate to serve as your point of contact, making sure you get to independent IRB approval as efficiently as possible.
From managing day to day tasks to handling issues if they arise, you can count on your Univo IRB associate for:
- Direct access to IRB expertise
- Clear and timely communications
- Accelerated IRB startup
- Guidance on submission process and IRB expectations
- Early identification of IRB documentation expectations
- Liaison to IRB regulatory support and guidance
Easy-to-Use IRB Technology
OneVerse is the only purpose-built IRB platform for central IRB review. Unlike dated systems that have been modified from decades-old, single-site research technology, it enables the highest efficiency of virtual workforces so you can enjoy superior service.
An industry-leading 21 CFR Part 11 compliant, electronic IRB submission portal, OneVerse supports:
- Transparency in submission and review decisions
- Direct communication chat to live resources
- Searchable resources
- Modern uploading and APIs
- Limited system training needed for end users
- Secure document sharing and collaboration
- 24/7 access from any type of device
Agile Solutions for Streamlined Independent IRB Approval
There are plenty of pain points in clinical research, but your IRB review process does not need to be one of them. Driven by a passion to enhance clinical research for the benefit of patients everywhere, we work tirelessly to understand and address your study’s complexities while mitigating risks and challenges to the patients.
Whether you’re running a Phase I healthy volunteer or a complex, Phase 3 interventional trial, our agile solutions and forward-thinking approach make IRB review simple and helpful.
Research Review
Running a trial in Canada?
Our Canadian Research Ethics Board (REB) is here to help! Get in touch to learn more.
Regulatory Consultation
Federal regulation requirements are complex. With 60+ years of IRB experience, we have the expertise you need to remain confidently compliant on your journey to independent IRB approval and beyond.
Our regulatory consulting services include:
- Informed consent preparation
- Prescreening protocols and consent
- Direct-to-patient decentralized trials
- Good clinical practice (GCP) audits
- FDA inspection preparation
- Investigator, CRA, and CRC training
Is your need not listed?
Get in touch with our team so we can customize a solution.
With fair pricing, innovation, and integrity, Univo IRB is the right choice for streamlined independent IRB approval.
