Outsource CRO Clinical Research Organization

Providing only outsource services

GO TOGO TO

Always look on the
bright side of life with
HEALTHY!

Our Values

Our Mission

To advance clinical research by delivering high‑quality, compliant, and efficient solutions that support sponsors throughout the clinical trial lifecycle, while prioritizing patient safety and data integrity

Our Commitment

We are committed to scientific integrity, regulatory excellence, and transparent collaboration—ensuring reliable results, patient‑centered conduct, and sustainable partnerships.

Regional Clinical Research Coverage

EBM provides high-quality, compliant clinical research services to global and local sponsors across Türkiye, the Middle East, and West Asia, supporting pharmaceutical, biotechnology, and medical device development with strong regional expertise

About Us

EBM CRO

EBM CRO is a clinical research services provider supporting pharmaceutical, biotechnology, and medical device companies, as well as global and regional CROs, across the full clinical trial lifecycle. By combining international standards with strong local expertise, EBM delivers compliant, efficient, and strategically driven clinical research solutions

Built on extensive experience within global CRO and pharmaceutical environments, EBM CRO bridges global clinical research expectations with deep local regulatory and operational knowledge.

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Patients served
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Therapeutic Experience
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Years of Sector Experience

THERAPEUTIC AREA EXPERTISE

EBM delivers clinical research services across a wide range of therapeutic areas, supporting Phase I to Phase IV drug and medical device studies. Our experience spans both common and complex indications, driven by globally experienced, locally specialized teams with a strong focus on patient safety, data quality, and regulatory compliance.

Key Therapeutic Expertise

Oncology

Early- and late-phase oncology trials requiring complex protocols, intensive monitoring, and strict patient safety oversight.

Hematology

Complex hematology studies involving high-risk patient populations and stringent safety and data monitoring requirements.

Rare Disease

Studies involving limited patient populations, specialized site coordination, and high regulatory and operational complexity.

Infectious Diseases

Acute and chronic infectious disease trials requiring rapid execution, strict compliance, and robust safety management.

Immunology

Clinical trials in immune-mediated and inflammatory diseases, including biologics and advanced therapeutic approaches.

Therapeutic Expertise

Cardiology
Clinical studies addressing cardiovascular outcomes, chronic conditions, and long-term patient management.

Dermatology

Clinical research in inflammatory, autoimmune, and chronic dermatological conditions across multiple study phases.

Diabetes

Metabolic and endocrine studies focusing on long-term disease management and patient adherence.

Gastroenterology

Clinical trials in inflammatory bowel diseases, functional gastrointestinal disorders, and chronic GI conditions.

Internal Medicine

Multi-indication clinical studies covering a broad range of systemic and chronic medical conditions.

Nephrology

Clinical trials in chronic kidney disease and renal disorders requiring specialized site and patient management.

Pulmonary Disease

Studies in respiratory conditions including chronic and progressive pulmonary diseases.

Rheumatology

Clinical research in autoimmune and inflammatory rheumatic diseases with long-term follow-up requirements.

Urology

Studies addressing functional and chronic urological conditions across diverse patient populations.

Psychiatry

Clinical trials in mental health conditions requiring patient-centered approaches and strict protocol adherence.

Physical Therapy

Interventional and observational studies evaluating functional outcomes and rehabilitation strategies.

Vascular Disease

Clinical research focusing on vascular disorders and cardiovascular-related interventions.

Wound Care and Healing

Studies evaluating wound management, tissue repair, and healing outcomes in complex patient populations.

Ophthalmology

Clinical trials in ocular diseases requiring precise assessments and specialized diagnostic methodologies.

Medical Imaging

Device-focused and diagnostic imaging studies supporting accurate data collection and interpretation.

This broad therapeutic expertise enables EBM to deliver both routine and complex clinical studies with confidence, flexibility, and a strong commitment to patient safety.

Compliance, Quality & Certifications

At EBM, quality, compliance, and data security are integral to every clinical research activity we conduct. Our operations are supported by internationally recognized certifications and industry memberships, reflecting our commitment to regulatory excellence, patient safety, and data integrity.

Quality
Management System

Information Security
Management System

Active member of
the Turkish Clinical Research Association

SOP & Internal Quality System

EBM operates under a comprehensive set of internally developed and regularly updated Standard Operating Procedures (SOPs) that govern all clinical research activities. Depending on project requirements, EBM SOPs may be applied alongside sponsor or global CRO SOPs to ensure standardized processes, regulatory compliance, quality control, and effective oversight across all studies.

CORE PARTNERS & KEY VENDORS

EBM collaborates with key partners and core vendors that play a critical role in clinical trial execution. These partnerships support strategic decision-making, regulatory compliance, and the delivery of high-quality clinical research across all study phases.

GLOBAL CRO Partners

EBM acts as a trusted local partner for global CROs, supporting regional study execution in compliance with international GCP standards and local regulatory requirements.

Pharmaceutical Companies

EBM provides end-to-end clinical research support to pharmaceutical sponsors, ensuring regulatory compliance, operational excellence, and reliable data generation.

Medical Device Companies

We support medical device manufacturers in conducting compliant clinical investigations for both CE-marked and non-CE-marked devices, including pre-market and post-market studies, in alignment with applicable regulatory requirements.

Contract Negotiation & Budget Management

EBM provides advanced contract negotiation and budget management capabilities, acting as a strategic partner to sponsors by managing complex site negotiations, optimizing study budgets, and maintaining full financial transparency and regulatory compliance throughout the study lifecycle.

Training & GCP Education

EBM delivers structured training programs to clinical research teams and study stakeholders, supporting GCP compliance, regulatory awareness, and consistent study conduct.

SUPPORTING & SPECIALIZED VENDORS

EBM works with carefully selected supporting vendors to deliver specialized services in compliance with regulatory and quality requirements.

TRANSLATION SERVICES

Certified translation vendors provide accurate, consistent, and regulation-compliant translations of clinical and regulatory documents in line with applicable local and international requirements.

PHARMACY SERVICES

Authorized pharmacy vendors support the compliant procurement, storage, dispensing, and tracking of investigational and standard-of-care products in accordance with national regulations.

LICENSED DEPOTS

EBM collaborates with regulatory authority–approved licensed depots to ensure compliant storage, handling, and distribution of investigational medicinal products.

HOME HEALTHCARE SERVICES

Qualified home healthcare providers support decentralized and patient-centric study activities, including home visits and protocol-required assessments, where applicable.

IMAGING CENTERS

Accredited imaging centers support protocol-driven diagnostic imaging and endpoint assessments in accordance with study-specific and regulatory requirements.

What People Usually Asked

EBM is a clinical research services provider supporting pharmaceutical, biotechnology, and medical device companies, as well as global CROs, across the full clinical trial lifecycle. With a highly experienced team combining global standards and strong local expertise, EBM delivers compliant, efficient, and strategically driven clinical research solutions in Türkiye and the surrounding regions.

EBM provides comprehensive clinical research services covering Phase I to Phase IV clinical trials, observational prospective and retrospective studies, and medical device clinical investigations. Our services include feasibility assessments, regulatory and ethics submissions, site management activities, study design, medical writing, data and biostatistics services, project management, quality assurance, and clinical research training—delivered in alignment with international and local regulatory requirements.

EBM’s clients include pharmaceutical, biotechnology, and medical device companies; global and regional CROs; academic research centers; and healthcare organizations seeking reliable clinical research expertise and local regulatory support.

EBM ensures research quality through a robust quality management framework supported by standardized processes, regulatory compliance, and continuous oversight. Our activities are governed by internal SOPs aligned with international standards, complemented by independent audits, quality controls, and experienced clinical research professionals to ensure data integrity, patient safety, and reliable outcomes.

To discuss potential collaboration or request clinical research services, please contact EBM using the details below.