You need to get IRB approval to meet your deadlines, but IRBs have become too big and bureaucratic, distracting them from their core responsibility to protect the rights and welfare of research participants.
Partner with Univo IRB for the participant-centered, high-touch service and forward-thinking technology that your study needs to meet timelines and navigate a changing industry.
Exceptional Service
Univo IRB is comprised of professionals who have either been research participants or have experience in human research.
With hospitality woven into our company DNA, we go above industry standards in our collaboration, increasing visibility and decreasing ambiguity to ensure participant safety and compliance every step of the way.
Our services include:
- 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
Single Point of Contact
Unlike at other IRBs 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 and your project are valued regardless of size.
From managing day to day tasks to handling issues if they arise, you can count on your Univo IRB associate for:
- 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 Technology
Lengthy submission forms, repetitive questions, clunky communication, and avoidable mistakes are in the past. Our technology 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, our system enables seamless study submission.
An industry-leading 21 CFR Part 11 compliant, electronic IRB submission portal, our platform 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
There are plenty of pain points in clinical research, but your IRB review 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 noninterventional online trial, our agile solutions and forward-thinking approach make IRB review simple and helpful.
Research Review
Is your study type or IRB need not listed?
Get in touch with our team so we can customize a solution to meet your needs.
Regulatory Consultation
Federal regulation requirements are complex. With 60+ years of IRB experience, we have the expertise you need to remain confidently compliant.
Is your regulatory consulting need not listed?
Get in touch with our team so we can customize a solution.
The Univo IRB Difference
With competitive pricing, innovation, and integrity, Univo IRB is the right choice for streamlined IRB research approval.