Independent. Rigorous. Inspection-Focused.
VIGIVANCE assesses, strengthens and maintains GCP/GVP quality systems, keeping clinical and pharmacovigilance operations audit-ready by design.
Independent audit and compliance support to assess, strengthen and maintain GCP/GVP quality systems and regulatory readiness across clinical and pharmacovigilance operations.
9 Audit Capabilities
Every engagement is carried out independently, against current regulatory expectation, with findings translated into a clear, actionable path to closure.
Independent GVP, GCP and PV system audits give an honest, evidence-based view of where your quality systems stand, separate from your own operational team.
The same rigorous audit standard is extended to vendors, service providers, affiliates and partners, so oversight stays consistent across your full network.
GAP, compliance and SOP assessments are translated into a prioritised CAPA plan, with follow-up tracked through to verified, inspection-ready closure.
Our GVP and GCP audits are carried out independently of your operational team, giving an honest, evidence-based view of where your quality systems stand.
Vendor and affiliate audits follow the same rigorous standard, so oversight extends consistently across every partner in your network.
We run GAP and compliance assessments against current regulatory expectation, then translate findings into a clear, prioritised CAPA plan.
Follow-up tracking continues through to verified closure, so corrective actions are confirmed effective, not just logged as complete.
Independent, Inspection-Focused Audit Support
Audit & compliance capabilities keeping quality systems inspection-ready by design.
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