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  • 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
Why do the new consent forms look different?
2
Do I need to revise my 1572 when WIRB is no longer in Olympia?
3
Is my protocol exempt from review?
4
Are Investigator’s Drug Brochures approved?
5
Can I submit paperwork before choosing a PI?