Case Study: CenExel Clinical Research achieves faster study startup and reliable ICF delivery with Advarra's ICF writing and IRB services

Large Clinical Research Site Network Streamlines Study Startup with Reliable, Timely ICF Writing Services

CenExel Clinical Research, a large clinical research site network, needed a new partner to write informed consent forms (ICFs) after their prior vendor stopped offering the service. With a heavy pipeline of Phase I trials and strict IRB requirements, CenExel required reliable, rapid ICF turnaround and writers familiar with IRB expectations; they turned to Advarra for ICF writing services (and coordinated IRB support).

Advarra implemented its ICF writing services through the CIRBI platform, working from whatever sponsor materials were available and aligning drafts with IRB policies to minimize back-and-forth. As a result, Advarra delivers compliant ICFs in as little as 2 business days, shortened IRB submission timelines, and enabled faster study startups and site initiation visits — becoming CenExel’s preferred ICF-writing and IRB partner and rolling the service out to additional sites.

CenExel Clinical Research