Research Site Network Enhances Study Startup With Reliable ICF Writing Services

To create informed consent forms (ICF) for clinical research, one must comprehend the protocol and regulations while investing ample time to ensure compliance and clarity. For CenExel Clinical Research, a large clinical research site network, this task was outsourced for their studies to maximize efficiency. However, their current vendor was no longer able to provide this service.

With many Phase I trials in the pipeline, CenExel Clinical Research sought a new informed consent form (ICF) writing partner with reliable, rapid turnaround times and that was familiar with its institutional review board (IRB) requirements. According to CenExel, previous vendors failed to meet the needs for prompt ICF delivery, while engaging vendors not affiliated with the study's IRB of record introduced further issues, as the ICF writer lacked knowledge of its specific requirements.

To address these issues, the team at CenExel began using Advarra’s ICF writing services for their studies. Discover how with Advarra’s ICF writing services and the organization’s IRB services, CenExel was able to streamline its processes and enable its team to start new studies faster.