CROs live between sponsors, sites, and inspectors. Spreadsheets that worked at five studies break at fifteen, and the enterprise CTMS packages built for large sponsors come with implementations a mid-size CRO can't justify. LabRelations takes a different approach. Our CTMS and QMS platforms are designed for how CRO teams actually work: multiple sponsors, standardized CRA workflows, site qualification, and a TMF that stays current as the trial runs. There's still setup, and our team is with you through it - but we've done the hard work upfront so you're operational sooner, with less complexity to manage across the portfolio. Both platforms are built to be intuitive, keeping clinical and quality teams productive and inspection-ready under GCP and 21 CFR Part 11.
LabRelations Clinical Platform is built for how CROs run studies and how they prove it to sponsors.
We're replacing spreadsheets and email with a single source of truth across the studies you run for sponsors. CTMS for studies, sites, subjects, and milestones. Standardized monitoring and CRA workflows. Site qualification and permit management. eTMF that fills itself as the trial runs, so close-out isn't a document hunt. Sponsors get the oversight they expect without you maintaining a parallel reporting stack.
A mix of people who've worked at CROs (usually clinical operations, oversight and monitoring) backed by technical people for configuration needs inside the platform itself. They know what a CRA visit report looks like, and they don't expect you to staff an IT department to go live.
