Your Trusted Partner in Global Clinical Research

Lanmer CRO connects European precision with regional expertise — streamlining the pathway from discovery to delivery through compliant, efficient, and high-quality clinical operations.

We are a European full-service CRO driven by a seasoned team of regulatory, operational, and medical experts experienced in managing complex multinational trials. Our team’s hands-on knowledge of EU and regional regulatory frameworks allows us to navigate complex environments with agility, ensuring smooth trial execution and dependable results.

Pan-European Reach. Regional Insight. Global Standards

Headquartered in Estonia, Lanmer CRO operates across all EU member states, the Balkans, and expanding regions from Türkiye to the Middle East and Africa through trusted partnerships and experienced local teams.

This network enables sponsors to conduct compliant, cost-efficient, and well-managed clinical trials across diverse populations and healthcare systems — from EU CTR-regulated studies to non-CTIS territories requiring tailored regulatory strategies.

Lanmer CRO connects European precision with regional expertise — streamlining the pathway from discovery to delivery through compliant, efficient, and high-quality clinical operations.

We are a European full-service CRO driven by a seasoned team of regulatory, operational, and medical experts experienced in managing complex multinational trials. Our team’s hands-on knowledge of EU and regional regulatory frameworks allows us to navigate complex environments with agility, ensuring smooth trial execution and dependable results.

Key Capabilities
  • Full-Service Clinical Trial Management – from feasibility and submissions to close-out

  • Regulatory Expertise – EU CTR / CTIS, GMP, GDP, GCP, and XEVMPD submissions

  • Multi-Regional Operations – EU, Balkans, Türkiye, MENA, and Sub-Saharan Africa

  • Therapeutic Breadth – biotechnology, pharmaceuticals, and medical devices

  • Local Networks, Global Oversight – harmonizing cross-border studies with centralized coordination

Lanmer CRO combines expertise, innovation, and a commitment to excellence to help you achieve your clinical research goals with precision and success.

Why Choose Lanmer CRO?
  • EU-Wide Compliance: Robust understanding of European and local regulatory landscapes

  • Strategic Flexibility: Adaptable models for single-country or multinational trials

  • Integrated Expertise: Combining regulatory, operational, and medical insight

  • Regional Strength: Deep local partnerships ensuring smooth delivery in emerging regions

  • Proven Execution: Reliable study management from start-up to reporting