Service → Milestone → Deliverable

Quality assurance, milestone by milestone

Select a milestone to see what we deliver at that point in the program.

Why NoyMed

Oversight built to hold up under scrutiny

Anyone can run a checklist audit. Sponsors choose the team behind it — how well findings are directed by real risk, how fast CAPAs close with evidence behind them, and how few surprises show up at the real inspection.

Findings that close

Audit and inspection findings feed directly into CAPA tracking, closing the loop through one process rather than a separate one.

Risk-based, not blanket

Oversight directed by the risk-based audit plan to where trial risk is highest, aligned with the site management team's monitoring plan.

Built for scrutiny

Documented, defensible processes that hold up under sponsor and health authority review, backed by biostatistics and data teams when findings touch study data.

Root cause, not symptom

CAPAs are built on a documented root cause analysis, not a quick fix that lets the same finding recur next audit.

Inspection-ready by design

The TMF and QA documentation are audit-traceable throughout conduct, not assembled under pressure before the real inspection.

Auditors who understand the data

Findings come with practical corrective paths because the same auditors understand both the operational and data sides of a trial.

Beyond the standard deliverables

Additional quality assurance capabilities

Structural QA support that doesn't map to a single milestone.

Quality management systems

QMS design & maintenance — the risk-based oversight structure every audit and CAPA runs on.

What sponsors say

Feedback we hear most

Common questions

Before you reach out

What sponsors typically ask before handing over their QA program.

Ready to talk about your QA program?

Tell us your study phase, vendor landscape, and timeline — we'll walk through how our QA team plugs in.