One safety record
The same team runs case processing and reconciliation — no data handoff between them.
Service → Milestone → Deliverable
Pharmacovigilance, milestone by milestone
Select a milestone to see what we deliver at that point in the safety lifecycle.
Why NoyMed
Safety data built to hold up under scrutiny
Every vendor can log a case. Sponsors choose the team behind it — how fast SAEs get reconciled, how defensible the signal evaluation record is, and how clean the safety database is at lock.
Built for scrutiny
Signal evaluation and reporting decisions are documented and defensible under sponsor or agency review.
Connected across the trial
Feeds directly into biostatistics, regulatory affairs, and medical writing — no reconciliation step.
Reconciled, not just reported
SAE reconciliation runs on an agreed cadence throughout conduct, not scrambled together before database lock.
Timelines that hold
SAE reporting workflows and site training are built and tested before go-live, so expedited timelines are never a scramble.
Inspection-ready archival
Safety plans, case records, and reports retained and traceable — see inspection readiness for how we prepare the full package.
Beyond the standard deliverables
Additional pharmacovigilance capabilities
Safety support that doesn't map to a single milestone.
Medical coding
MedDRA and WHODrug coding applied consistently across the case series, alongside case processing.
What sponsors say
Feedback we hear most
Common questions
Before you reach out
What sponsors typically ask before handing over their safety database.
Ready to talk about your safety database?
Tell us your study phase, safety database platform, and timeline — we'll walk through how our safety team plugs in.