One team, no handoff
Site data flows straight into our biostatistics and data management teams — no reconciliation between vendors.
Service → Milestone → Deliverable
Select a milestone to see what we deliver at that point in the study.
Why NoyMed
Anyone can schedule a monitoring visit. Sponsors choose the team behind it — how realistic the feasibility assessment was, how fast a site issue gets resolved, and how clean the TMF is when the site closes.
Site data flows straight into our biostatistics and data management teams — no reconciliation between vendors.
Monitoring and documentation practices aligned with quality assurance standards, ready for audit.
Site activation is coordinated with the same team running clinical trial management, so timelines stay realistic from day one.
Site selection is screened against real enrollment potential, not just investigator interest — fewer sites activated that never enroll.
Site issue escalation runs to documented resolution, not an open ticket that resurfaces at the next visit.
Essential document reconciliation and payment closure run before the close-out visit, not scrambled after it.
Beyond the standard deliverables
Operational and specialized support that doesn't map to a single milestone.
Day-to-day trial management across timelines, budgets, and vendors, with one accountable point of contact.
End-to-end operational oversight, integrated directly with our Biometrics division.
Visits and reviews concentrated where risk actually is, layered on top of the standard monitoring cadence.
Remote visits and connected device data coordinated alongside conventional site activity.
Use-related risk testing for devices, from formative research through summative validation.
What sponsors say
Common questions
What sponsors typically ask before handing over site management.
Tell us your target sites, therapeutic area, and timeline — we'll walk through how our site management team plugs in.