THE ONLY GLOBAL STANDARD
FOR CLINICAL RESEARCH SITE QUALITY AND SAFETY
From the participant in a clinical trial to the patient receiving
treatment from a physician, the measures of "safe and effective" begin at the trial site. The SASI-QMS:2023-2 Standard
is grounded in GCP, focused on QM fundamentals and work culture, and is a benchmark for CRS operations. The
3-Step SASI Accreditation process is a pathway to success.
Step 1: Complete the Exploratory Program.
Step 2: Take the "SASI Pledge for Quality and Safety," and as you prepare for accreditation, market your CRS to Sponsors,
IRBs, or potential trial participants with a link to your SASI Pledge Page on our website.