Empowering Clinical Research Across Europe and Emerging Regions
Lanmer CRO delivers comprehensive, end-to-end clinical research services — connecting European regulatory precision with regional operational excellence across the EU, Balkans, Türkiye, and Africa.
Our Core Services
- Clinical Trial Management – Full lifecycle management from feasibility and site selection to close-out, ensuring efficiency, transparency, and compliance.
- Regulatory Support – Expert navigation of EU CTR/CTIS, GMP, GDP, and local regulatory pathways for both drug and non-drug studies.
- Medical Writing – Development of clear, compliant, and submission-ready documents including protocols, IBs, IMPDs, DSURs, and clinical study reports.
- Patient Recruitment & Retention – Localized strategies leveraging strong site relationships and population insights to meet enrollment goals.
- Site & Investigator Support – Continuous communication, training, and monitoring to ensure site engagement and protocol adherence.
- Quality Assurance & Compliance – Internal and external audit capabilities ensuring adherence to GCP, ISO, and sponsor requirements.



