Featuring: WIRB’s NIH Single IRB Review Solution

WIRB NIH Single Review Solution

Making it easy for Academic Medical Centers and investigators to comply with NIH’s Single IRB policy.

  • Gold standard review service
  • IRB budgeting tools and SmartForms for NIH grants
  • Letter of support for grant submissions
Why WIRB for NIH Grants

The chosen IRB partner to over 175 contracted Academic Medical Centers.

  • Single IRB process that is 100% compliant with NIH requirements
  • Coordinates IRB submissions with participating investigators and local IRB offices
  • Customized approach to each and every participating site
How WIRB Serves As The Single IRB

Start up faster, enroll sooner, collect data quicker.

  • Rapidly assist in developing annual, ready-to-submit budgets
  • Customized ICF template for each site
  • Assistance coordinating submissions with sites

RESOURCES

TRUST THE PROVEN EXPERTS

First independent review board founded in
1968

Trusted partner to over
2,700
contracted institutions
in the United States

175+
contracted Academic
Medical Centers in our network
of affiliates

ISO 9001:2008
certified, meeting rigorous
quality management
standards

8
individual AAHRPP-accredited
review panels

Employs over
150
experienced board members

50
years of experience in protocol
& study-related review

 Longest accreditation history
of all IRBs – first accredited in
2003

e-Consent for NIH-Sponsored Clinical Trials

WCG’s ConsentNow™ (formerly Patient Genesis) offers an affordable and seamless way to create, share, and transfer knowledge to patients during the informed consent process. Institutions that use WIRB’s Single IRB Solution for NIH sponsored clinical trials enjoy automatic and convenient documentation, along with a higher level of consistency in the informed consent process in comparison to paper-based consent.

Request a Demo

Get in touch to ask questions or to get
started using this service

singlereview@wirb.com

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