One team, no handoff
The same programmers who build your datasets work from the SAP written in Biostatistics — nothing lost in translation.
Service → Milestone → Deliverable
Statistical programming, milestone by milestone
Select a milestone to see what we deliver at that point in the study.
Why NoyMed
Programming built to hold up under scrutiny
Every CRO can run SAS. Sponsors choose the team behind it — how clean the SDTM/ADaM lineage is, how few Pinnacle 21 findings survive to submission, and how directly the TLFs drop into the CSR.
Clean data in
Programming starts from data already checked by clinical data management, so fewer queries surface downstream.
Connected downstream
Datasets and TLFs feed straight into clinical study reports — no reconciliation step.
Independent double programming
Every dataset and key output confirmed by a second, independent program before it's called final — not a single-point-of-failure QC step.
Submission-ready by design
Define.xml, reviewer's guides, and Pinnacle 21 checks built alongside the datasets, not reverse-engineered before filing.
Inspection-ready archival
Programs, logs, and outputs retained and traceable — see inspection readiness for how we prepare the full package.
Beyond the standard deliverables
Additional statistical programming capabilities
Programming support that doesn't map to a single milestone.
TLF dry runs
Mock TLFs run early against interim or simulated data to catch programming issues well before database lock.
What sponsors say
Feedback we hear most
Common questions
Before you reach out
What sponsors typically ask before handing over their programming workstream.
Ready to talk about your programming workstream?
Tell us your study phase, CDISC standards version, and timeline — we'll walk through how our programming team plugs in.