To stay on track and maintain compliance, clinical trial regulations require the secure and timely exchange of critical safety reports between clinical safety departments, CROs, institutional review boards, and investigators. Yet most life sciences companies still perform this distribution manually and incur per-report costs that add up to staggering costs in labor, paper and postage.
The time has come to overhaul a time-critical responsibility and favorably impact your company’s compliance, and bottom line. Watch this 30-minute on-demand webinar to learn how companies can:
- Significantly reduce the associated costs and workload burden of safety report distribution
- Facilitate regulatory compliance during clinical trials
- Transform manual, labor-intensive processes into an integrated, automated solution, configurable to your business requirements