Regional Expertise. Global Standards.

Lanmer CRO delivers full-service clinical research and regulatory support across Europe, the Balkans, Türkiye, and Africa, combining European precision with regional operational excellence.
Our experienced teams and trusted partners ensure smooth trial delivery, full regulatory compliance, and measurable results across diverse healthcare systems and populations.

Operational Model

We operate through a centralized oversight structure supported by local experts in each country, enabling consistent quality, agile communication, and regulatory accuracy.
This model ensures seamless management of EU CTR/CTIS studies, MDR/IVDR submissions, and non-CTIS territories, all under unified project control.

Scientific, Clinical & Regulatory Expertise

Lanmer CRO supports a broad range of therapeutic areas and study types — from early feasibility to large-scale pivotal trials — as well as medical device and diagnostic investigations under EU MDR and IVDR.
Our multidisciplinary expertise ensures each program meets the highest regulatory and scientific standards, facilitating market access and CE certification across Europe.

Comprehensive advisory services
Why Sponsors Choose Lanmer CRO

  • Integrated EU & Regional Coverage – One partner for all European and emerging markets

  • Regulatory Mastery – End-to-end expertise in CTR, MDR, IVDR, CE-marking, and XEVMPD

  • Flexible, Scalable Models – Adapting to sponsor, protocol, and country requirements

  • Experienced Leadership – Senior professionals with multinational trial experience across drug and device programs

  • Commitment to Excellence – Delivering precision, compliance, and innovation in every project

Lanmer CRO — European Excellence. Global Reach. Proven Results.

Ready to bring your product to market?

Partner with Lanmer CRO to accelerate your path from clinical development to regulatory approval — efficiently, compliantly, and with confidence.