Feasibility
Country and site feasibility with recruitment potential and startup constraints. This workspace exists to enforce consistent clinical execution with accountable ownership, governed evidence, and inspection-ready traceability across the study lifecycle. It supports business and regulatory requirements by connecting operations, quality, submissions, and financial controls in a single system where handoffs are explicit and auditable. Users can proceed by filtering scope, reviewing linked artifacts and actions, and routing escalations with defined approval gates and signature meaning.
Feasibility Follow-Ups
| Item | Details |
|---|---|
| FEAS-1700 | US | Recruitment confidence 72% | PI availability high |
| FEAS-1701 | CA | Recruitment confidence 73% | PI availability medium |
| FEAS-1702 | GB | Recruitment confidence 74% | PI availability high |
| FEAS-1703 | DE | Recruitment confidence 75% | PI availability medium |
| FEAS-1704 | FR | Recruitment confidence 76% | PI availability high |
| FEAS-1705 | ES | Recruitment confidence 77% | PI availability medium |
| FEAS-1706 | IT | Recruitment confidence 78% | PI availability high |
| FEAS-1707 | NL | Recruitment confidence 79% | PI availability medium |
| FEAS-1708 | BE | Recruitment confidence 80% | PI availability high |
| FEAS-1709 | SE | Recruitment confidence 81% | PI availability medium |
Access & Governance Controls
Operational Controls
Study firewalling chips highlight boundary, country constraints, and vendor partition rules.
Actions requiring GxP control include a human review checkpoint and e-signature meaning capture.
Every state change writes immutable audit evidence with actor, timestamp, and object reference.
Next Actions
Filter to portfolio/program/study context.
Open linked tasks, risks, and document evidence.
Escalate blocked items through governed workflow.