Our services
Expertise, Applied Across the Product Lifecycle.
Pharmacovigilance at the core, with connected expertise around it
VIGIVANCE brings together specialized pharmaceutical capabilities across safety, regulatory, clinical, medical and quality disciplines, designed to provide depth where it matters and continuity across the lifecycle.
Pharmacovigilance
Safety, Structured. Oversight, Continuous.PV System Establishment & Governance · QPPV & Local PV Oversight · Safety Information Management · Safety Reporting→Regulatory Affairs
Strategy, Submission. Lifecycle, Continuity.Regulatory Strategy & Intelligence · Product Registration & Market Authorisation · Post-Approval & Lifecycle Management · Regulatory Submissions & Documentation→Medical Writing
Scientific Depth. Regulatory Precision.Clinical Documentation · Safety & Pharmacovigilance Writing · Regulatory Writing · Clinical & Non-Clinical Reports→Clinical Study Project Management & Support
Coordinated Execution. Controlled Delivery.Study Feasibility & Planning · Site Start-Up & Initiation · Study Operations & Coordination · Monitoring & Site Oversight→Audit & Compliance
Assurance Built Into the System.Quality System Assessment · GVP & PV Compliance · Audits & Assessments · Gap Assessment & Remediation→From individual services to integrated support
One partner. One coordinated framework. Multiple areas of expertise.
A client may engage us for pharmacovigilance alone. Another may need regulatory affairs and medical writing. A clinical study may combine clinical study project management with medical writing. The advantage stays the same.
Single function
One service, full depth
Specialized support for a defined functional requirement.
Combined
Complementary services
Two or more services that share information and timelines.
Integrated
Cross-functional scope
Multiple functions under one governance and delivery structure.
Not sure which services you need?
Share your requirement and we will recommend the right combination.