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WIRB SERVICES
IRB Services
Clinical Pharmacology Unit Review
Institutional Biosafety Committee
Data Safety and Monitoring
Education and Consulting
Global Services
With human lives at stake, trust the proven experts
For more than 40 years
, WIRB has been at the forefront of protecting the rights and welfare of human subjects. We provide indepth regulatory expertise to support your development of research protocols and documentation.
We offer customized training and consulting about human protections, addressing research design through implementation. And, we deliver unparalleled review quality to ensure your research withstands scrutiny around the world.
Learn more about the WIRB advantage.
IRB Services
Regulatory requirements, multi-site coordination, institutional needs—there are many complexities that can slow down research. With our unparalleled regulatory insight and experience, WIRB can manage these complexities and ensure your research gets a thorough review quickly.
Learn more about our IRB Services.
Clinical Pharmacology Unit Review
The clock is always ticking for clinical pharmacology research. WIRB's Clinical Pharmacology Unit Services division is set up to respond quickly for fast and thorough review of Phase 1 studies and beyond.
Learn more about CPUS reviews.
Institutional Biosafety Committee
Safe storage, handling, and disposal of gene-modified, biohazardous materials-these issues are among the many challenges for investigators and sponsors of research involving recombinant DNA. WIRB's Institutional Biosafety Committee Services (IBCS) can help your team navigate this complicated issue and protect the safety of staff, communities, and the environment.
Learn more about IBCS.
Data Safety And Monitoring
Double-blind studies, conflicts of interest, unintentional bias—there are many reasons why sponsors and investigators might seek to shield themselves from results in progress. Our Data and Safety Monitoring Services (DSMS) provide the outside clinical analysis and judgment researchers depend on when they need independent monitoring of emerging results.
Learn more about DSMS.
Education and Consulting
Improve your ability to maintain compliance and protect human subjects with guidance from our experienced educators and consultants. We offer a wide array of training, consulting, and staffing services for investigators, institutions, and sponsors. WIRB can help you write your protocol or your consent form, provide regulatory support for local IRBs, and deliver insights about IBCS issues.
Learn more about our Education and Consulting Services.
Global Services
With review experience in more than 70 countries, including Canada, WIRB can help you meet all the logistical, cultural, and regulatory challenges of international research. If you are planning an international study, WIRB's established international network and deep knowledge of global regulations and cultural sensitivities can help pave the way for a compliant review around the globe.
Learn more about our Global Services.
1968
WIRB opened its doors
2003
IRB accreditation from AAHRPP
20,000
active studies under WIRB oversight
News and Events Results
June 22, OHRP 2012 Community Forum
June 24-28 DIA 2012 Annual Meeting
June 1-5, ASCO 2012 Annual Meeting
Experts Corner Results
FDA August 2011 Draft Guidance: “Oversight of Clinical Investigations – A Risk-Based Approach to Monitoring”
New Requirements for Reporting Serious Adverse Events
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FREQUENTLY ASKED QUESTIONS
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WIRB “looks” different now. Why?
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