UK/EU QPPV

EU QPPV Oversight You Can Rely On

If you operate in the EU, you are required to have an EU QPPV who is visible, accountable, and inspection-ready at all times. Our EU QPPV service gives you experienced, regulator-facing oversight of your pharmacovigilance system, so you stay compliant with EU GVP requirements, maintain continuity of responsibility, and are prepared when regulators come calling.

Guided by the Rules. Trusted by Regulators.

When you appoint an EU QPPV, you need more than experience, you need confidence that your oversight reflects how regulators interpret and apply the rules. Our team has helped shape international pharmacovigilance guidance and brings that regulatory perspective directly into your EU PV system, so your approach stands up in real inspections, not just on paper.
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EU QPPV Responsibility Is Not Just a Role, It’s a Regulatory Risk

Maintaining effective EU QPPV oversight can be difficult as organizations grow and change. Gaps in accountability, availability, or escalation pathways are common inspection findings and can quickly increase regulatory risk. We help you maintain clear responsibility, consistent oversight, and alignment with EU GVP expectations.

Maintaining effective EU QPPV oversight can be difficult as organizations grow and change. Gaps in accountability, availability, or escalation pathways are common inspection findings and can quickly increase regulatory risk. We help you maintain clear responsibility, consistent oversight, and alignment with EU GVP expectations.

How We Support Your EU QPPV Responsibilities

Our Instant PV Department adapts to your needs via eight core pillars. We cover every critical function to ensure a high-performing, stress-free system.
Build a PV Department That Fits Your Timeline
Stop managing the burden of building from scratch. Get more information on our fully integrated modules and discover exactly how we stabilize your safety operations.

FAQ

How do I know if this service is the right fit for my situation?
Every iVigee service is designed to meet you where you are. Whether you’re building a PV function, stabilizing operations, or preparing for more complex change, the right fit depends on your products, timelines, and current pressures. When you reach out, we focus on understanding your reality first, not pushing a predefined solution. From there, we’ll help you determine whether this service makes sense now, later, or not at all.
Can services be tailored, or are they delivered as fixed packages?
Will iVigee work alongside our internal team and existing vendors?
What happens after I request information about a service?
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Here’s what working with us actually looks like

Understand Your Setup
We start by understanding your products, EU footprint, and current pharmacovigilance system. This allows us to confirm scope, responsibilities, and the level of EU QPPV oversight you need.
Establish EU QPPV Oversight
We appoint your EU QPPV, define responsibilities, and put the required governance, escalation pathways, and documentation in place, ensuring alignment with EU GVP requirements from day one.
Maintain Oversight and Inspection Readiness
Your EU QPPV provides ongoing oversight of your PV system, supports regulatory interactions, and helps keep your system inspection ready as your organization evolves.
No fluff. No surprises. Just clarity and accountability.

Practical resources to help you make better PV decisions

Explore practical tools, insights, and resources designed to help you make confident PV decisions at your own pace.
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