Why VAT Recovery in Clinical Trials Is Becoming More Complex
Clinical trials conducted across multiple jurisdictions often generate significant VAT embedded in CRO invoices, investigator and comparator payments, logistics, and site costs. Historically this VAT has been recovered through reclaim processes supported by supplier invoices. However, as electronic invoicing and real-time digital reporting expand across jurisdictions, VAT recovery increasingly depends on access to validated invoice data and correct supplier behaviour. Where these conditions are not met, VAT recovery can fail even when the underlying VAT should in principle be recoverable.
Our Core Services
EU VAT Eligibility Review
Identify reclaimable spend across EU clinical trial operations.
End-to-End Reclaim Filing
We handle the full reclaim process across multiple EU jurisdictions.
Compliance Support & Documentation
Light-touch audit readiness and document prep to stay compliant.
Why Finance Leaders Trust Clearview
Specialised in Life Sciences VAT
We focus exclusively on pharma and biotech firms operating in the EU.
Tailored, Low-Effort Process
Minimal lift for your finance team — we manage the reclaim end-to-end.
Performance-Based Pricing
No upfront cost. We only earn when you reclaim.
EU VAT Eligibility Review
Informed Recovery Starts with Eligibility
At Clearview Compliance, we understand that clinical trial operations across Europe often create hidden VAT recovery opportunities. Our EU VAT Eligibility Review helps finance leaders in non-EU pharmaceutical and biotech companies identify which trial-related expenses may qualify for reimbursement under the 13th Directive.
Targeted Analysis of EU Spend
We take a structured approach to reviewing your vendor invoices, service categories, and jurisdictional exposure. From CRO contracts to lab fees and investigator payments, we assess where your spend aligns with reclaimable VAT criteria - and where potential value may be going unclaimed.
A Service Tailored to Life Sciences
Every life sciences company operates differently, and so does their VAT profile. Whether you're a clinical-stage biotech with multiple EU trials or a niche pharma company working with local CROs, we tailor our review to your business model, trial footprint, and finance workflows.
Collaborative, Low-Effort Process
Our review process is fully managed and designed to minimise disruption. We work directly with your finance or operations teams to access only the documentation we need - then deliver a clear assessment of your reclaim potential and next steps.
Unlock Compliance-Aligned Recovery
Our Eligibility Review gives you clarity, confidence, and a starting point for recovering EU VAT that might otherwise be lost. We help you unlock cash flow while maintaining compliance with local tax regulations - all with no upfront fees.