From safety surveillance and regulatory submissions to quality oversight and delivery governance, VIGIVANCE brings five integrated service pillars together under one accountable team.
VIGIVANCE is a full-service partner delivering end-to-end pharmacovigilance, regulatory, medical writing, clinical and audit services. Our expertise spans multiple therapeutic areas and regulatory environments globally.
Each pillar is delivered by specialists in that domain, coordinated through a single point of accountability. Open a pillar to view its full capabilities.
Compliant, effective, inspection-ready safety systems across global markets.
Read the capabilities →Product registration, lifecycle management, and post-marketing compliance.
Read the capabilities →Rigorous documentation for submissions, safety evaluation, and clinical development.
Read the capabilities →Operational and scientific support aligned to regulatory and quality requirements.
Read the capabilities →Independent GCP/GVP audit support and inspection readiness.
Read the capabilities →What sets VIGIVANCE apart when you need a dependable, accountable pharmacovigilance and regulatory partner.
100+ countries of operational experience across markets and product types.
15+ Pharmacovigilance systems built and maintained for sponsors of every size.
20+ GVP audits and compliance assessments completed, start to finish.
Named, accountable oversight embedded into every engagement, never a shared inbox.
Structured workflows and safety technology built for data quality and full audit trails.
“Compliance assessment, GAP analysis, CAPA, and audit & inspection support are built into how we work, keeping PV and regulatory systems continuously inspection-ready.”
A multidisciplinary team of medical, scientific, and regulatory professionals bringing deep, hands-on pharmacovigilance and regulatory experience to every engagement.
Scope, governance, and delivery models shaped around your product portfolio, markets, and internal capabilities, never a one-size-fits-all package.
Continuous safety surveillance and signal management designed to identify and address risk before it becomes a compliance issue.
Support that spans development, market entry, post-authorisation, and beyond, a single partner across the full product lifecycle.
Our end-to-end pharmacovigilance capability, complemented by regulatory affairs, medical & scientific writing, clinical research support and independent audit & compliance services, enables us to support defined requirements across the pharmaceutical product lifecycle.
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