CROMNIA
Reliable Data • Flexible Services • Regulatory Excellence
Providing reliable clinical research services for Phase II–IV trials across all therapeutic areas in Turkey, in full compliance with ICH/GCP standards and the requirements of regulatory authorities.
Who We Are
Guiding principles behind every clinical research project we manage.
Our Mission
What We Do
To provide reliable data with the highest quality of our flexible and more cost-effective services on time, in accordance with requirements of Regulatory Authorities and with provisions of ICH/GCP.
Our Vision
Where We're Going
To develop and provide a wide range of clinical research services — from study design through site monitoring and administration to data analysis and medical writing — in compliance with clinical research requirements and working to the highest international professional and ethical standards.
Our Services
Comprehensive clinical research solutions from site selection through final reporting.
Why Choose CROMNIA
What sets us apart in the competitive CRO landscape.
ICH/GCP Compliant
Every project we manage adheres to International Council for Harmonisation (ICH) and Good Clinical Practice (GCP) standards — the global benchmark for clinical trial quality.
Established Since 2009
Over 15 years of deep experience in the Turkish and international CRO market, with a proven track record managing Phase II–IV clinical and observational trials.
Cost-Effective Solutions
Flexible service models designed to maximize sponsor budget efficiency without compromising data quality, regulatory compliance, or timelines.
Regulatory Expertise
Direct submission experience with Turkish regulatory authorities (MoH), Local Ethics Committees (LECs), and European regulatory frameworks.
Ready to discuss your next clinical research project?
Contact our team→