Image only in PDF
Review Services

Gene Therapy Ready Site Network

Key Benefits

  • Largest global network of NIH-registered sites
  • Faster study startup
  • No cost to join
  • IBC review in ≤10 business days

GTR Advantages

Faster Clinical Trial Startup

Network sites complete study startup 5-6 weeks faster than non-network sites, and 8-12 weeks faster than sites using a local institutional biosafety committee (IBC).

Comprehensive Site Support

Advarra works with network sites to ensure compliance with NIH and biosafety standards, reducing risks and making them more attractive to sponsors.

No Cost and No Commitment

Joining the network is free, with no obligations beyond maintaining biosafety compliance. This gives sites a competitive edge without added costs.

Complementary NIH Registration

Sites receive complimentary National Institutes of Health (NIH) registration when Advarra serves as the IBC of record. This simplifies the startup process, helps ensure compliance with NIH Guidelines.

Demonstrated Site Expertise

Membership demonstrates a site’s expertise and readiness to safely conduct trials involving genetically engineered therapies and vaccines. This attracts sponsors and proves site capabilities in handling complex gene therapy studies. This helps attract more industry-sponsored trials and proves the site’s commitment to biosafety best practices.

Turnaround Times

Sites in Advarra’s GTR Network are pre-registered with NIH to conduct research according to NIH Guidelines, have an existing IBC, and prior experience with human gene transfer studies. This results in significantly shorter review and approval times. When Advarra serves as both the central institutional review board (IRB) and IBC, network sites can often be approved in just a few days – dramatically faster than sites outside the network.

–6
weeks faster than non-GTR Network sites
–12
weeks faster than local IBC sites

Sites

Sponsors

Save as PDF
Scroll to Top