Compliance Support & Documentation
We help ensure your documentation is audit-ready and aligned with each EU country’s VAT reclaim requirements — so submissions are accepted, not rejected.
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.
Keeping You Compliant, Efficiently
Navigating EU VAT rules can be challenging — especially when you're running multiple clinical trials across different jurisdictions. At Clearview Compliance, we provide light-touch, practical support to help your team meet documentation and audit standards without unnecessary burden.
Aligning Documents with Local Requirements
Each EU member state has specific expectations for VAT reclaims — from invoice formatting to proof of payment and service detail. We review your documents before submission, flag missing items, and help you align with the local authority’s compliance criteria, reducing the risk of delays or denials.
Seamless Collaboration with Your Team
We work directly with your finance or clinical operations team to access only what’s needed — no endless checklists or audit-heavy processes. Our support is designed to be lean, responsive, and easy to integrate into your existing workflows.
Reducing Risk, Enhancing Confidence
Our compliance support gives you confidence that each reclaim is audit-ready, country-aligned, and complete. Whether you’re filing one reclaim or building a recurring process, we make sure your submissions are well-documented and defensible.