{"status":"OPERATIONAL","token_format":"TRL-{STUDYHASH8}-P{PARTICIPANTHASH6}","standards":["FDA 21 CFR Part 312 (IND)","21 CFR Part 11 (electronic records)","ICH GCP E6(R3)","ICH E2A (adverse event reporting)"],"fabric_channel":"consent-channel","use_cases":["Phase I-IV clinical trials","SBIR/STTR federally-funded research","Real-world evidence studies","NIH-sponsored studies"]}