• Overview
  • Sponsors/CROs
  • Institutions/Investigators
  • Submission Resources


Fast and efficient reviews

Regulatory requirements, multi-site coordination, institutional needs—there are many complexities that can slow down research. With our unparalleled regulatory expertise and experience, WIRB can manage these complexities and ensure your research gets a thorough review quickly.

Expertise
Seven review panels
Client portal
Quality services

View WIRB's Compliance Statement, and learn more about WIRB's registration with OHRP/FDA, AAHRPP accreditation, and electronic signatures' compliance with 21 CFR Part 11.

FREQUENTLY ASKED QUESTIONS
1
Can I submit paperwork before choosing a PI?
2
Where do I find re-consent instructions?
3
Why do the new consent forms look different?
4
Is my protocol exempt from review?
5
What do I need to know about WIRB's relocation to Puyallup?