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Est. 2009 · ICH/GCP Compliant

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.

By the numbers

Proven scale, measurable trust

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Years Experience

Operating in the Turkish CRO market since 2009.

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ICH/GCP Compliance

Every trial follows international quality standards.

Phase II–IV

Trial Coverage

From early efficacy through post marketing.

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Core Services

Project management to medical writing under one roof.

What we do

Our Services

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Site Selection and Feasibility

Comprehensive evaluation of investigator sites to identify the optimal locations for successful clinical trial execution.

Clinical and Observational Trial Management

End to end management of Phase II–IV clinical and observational research projects across all therapeutic areas.

Regulatory Affairs

Expert handling of all regulatory submissions and compliance requirements from Ministry of Health to Local Ethics Committees.

Medical Writing

Professional clinical documentation produced in collaboration with investigators and scientists across all therapeutic areas.

Site Coordinator Services

Dedicated on site coordinators supporting investigator sites with day to day trial operations and patient management.

Medical Translation

Precise, on time medical translation services delivered by a physician led team with deep clinical expertise.

Investigator Meeting Organization

Full service planning and execution of investigator kick off meetings, including logistics, travel, and presentations.

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

Ready when you are

Launch your trial with confidence

From feasibility to final report, let's discuss how CROMNIA can support your next clinical research program in Turkey.