The FDA’s Notice of Proposed Rule Making regarding the Single IRB mandate is coming. Are you ready? With WCG IRB, you can be. Our team of experts is ready to guide you through the process, ensuring your research is compliant and ready for the changes ahead.


Accelerate your Research

Of note for Sponsors & CROs, streamlining the consent process is a key part of the Single IRB mandate. The rewriting and approval process for your consent forms can be an arduous process. WCG has the expertise and experience to help you create a streamlined, compliant process that meets the needs of your research and protects your participants.


Take Control of your Study

Don’t get caught off guard. Take control of your research’s future today and speak with the experts at WCG IRB. Our team is standing by, ready to help you prepare for the FDA’s Single IRB mandate and streamlined consent process. If you’re looking to start a new study with WCG IRB, or transfer studies to us for review oversight, fill out the form below and a member of our team will be in touch shortly to help you get started.

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