The FDA's Single IRB Notice of Proposed Rule Making is fast approaching, and you need to be ready. WCG IRB understands the challenges that institutional IRBs face and is here to help.
We understand that no one understands your local population better than you. That’s why WCG belives in balancing compliance with flexibility – we assimilate your local Standard Operating Procedures while ensuring you meet the FDA’s upcoming requirements. Our experts understand local issues and bring a wealth of board knowledge to the table, ensuring excellent review of your clinical trials.
ARE YOU READY?
Say goodbye to the stress of navigating the Single IRB mandate on your own. WCG IRB is here to help you maintain compliance, minimize burden, and ensure the success of your IRB processes – all while opening the possibilities of increased exposure to clinical trial opportunities never before available.
Don’t wait until it’s too late. Contact WCG IRB today and get ready for the FDA’s Single IRB mandate with confidence.
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.