
1. Clinical trials and R&D collaborations
Clinical trials are tightly regulated from Phase I to Phase IV, and every step leaves a documentation trail.
- Store protocols, informed consent forms, monitoring reports, and DSMB documentation in structured folders.
- Share controlled access with investigators, CROs, labs, and regulators, with full traceability of who accessed which file.
- Support inspections and audits by keeping evidence and correspondence in one compliant, searchable workspace.


