Info Sheet

IBC Review and Consulting Services

Make your gene therapy research altogether better

Gene therapy research is on the verge of exploding. Study startup is already a challenging process—why add the complication of IBC reviews that take more than a month to complete?

No waiting for a standing meeting. No submission deadlines. Coordinated IBC and IRB reviews for added efficiency.

With a diverse roster of career biosafety professionals and a secure, user-friendly submissions platform, Advarra routinely performs IBC reviews in 10 business days or less from receiving a complete submission.

IBC Services:

  • IBC setup and registration support
  • Protocol review and approval
  • Education, training, and operations consulting
  • IBC compliance and management
  • Local IBC submission support
  • Coordinated IBC and IRB reviews
  • Complimentary IBC assessment of protocol
  • No-cost NIH registration for sites

Want more information on how Advarra can accelerate the regulatory approval process for your next gene therapy study? Fill out the form to download our info sheet.





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DATE
Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

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