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Türkiye Türkiye
Ukraine Ukraine

Türkiye is an up-and-comer in clinical research

With a population of over 85 million, a well-developed universal healthcare system, a relatively low per capita number of clinical trials, and a large pool of treatment-naive patients, Türkiye is a hidden gem in clinical research. In fact, the number of biotech and pharma companies that are getting engaged in Türkiye has been on the rise, with the  number of clinical trials doubling there for the last 3 years. Over the past two decades the country has steadily worked its way to establishing a strong reputation in the clinical trials segment. Today, these efforts are coming to fruition, as evidenced by the rising number of international companies looking at Türkiye for their next trials. 

Türkiye Quick Facts
1.9
doctors
(2019)
per 1 000 population
3
hospital beds
(2020)
per 1 000 population
86.6
millions
(2023)
Total population
1473
initiated clinical trials
in 2022
78.4
years
(2023)
Life expectancy
Main advantages of conducting clinical trials in Türkiye:
  • High number of enthusiastic physicians and dedicated clinical research staff
  • Modest number of trials per capita
  • Well-reputed research sites with strong technological infrastructure capabilities, on par with EU and US
  • Full compliance with GCP and international quality standards
  • Higher percentage of easily accessible, treatment-naïve patients interested in participating in clinical trials
  • Moderate clinical research costs and investigator fees
  • GMP certificate is sufficient for regulatory submissions and the EU QP Statement is not required

Cromos Pharma’s Services in Türkiye:

What we do

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Patient recruitment
Patient recruitment
  • Promotional and educational materials
  • DTC outreach
  • Investigator’s materials
  • Booster visits
  • Referral sites
  • Commitment to patients
  • Patient’s materials
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Clinical Research Services
Clinical Research Services
  • Capability and Feasibility Assessment
  • Project Management
  • Monitoring Services
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Regulatory
Services
Regulatory Services
  • Compilation of initial documents for RA and ECs/IRBs
  • Review of IC documentation
  • Obtaining of trial subjects’ insurance
  • Secure import/export licenses
  • Regional regulatory consultation
  • Regulatory strategy and clinical development planning
  • Submissions to Regulatory Agencies
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Medical
Writing
Medical Writing
  • Study concepts and outlines
  • Clinical study protocols and amendments
  • SAP for inclusion into protocol
  • Investigator Brochures
  • Investigational Medicinal Product Dossiers
  • Patient Informed Consent Forms
  • Clinical Study Reports
  • Executive summaries for efficacy or safety, ISS, ISE
  • Reviews of clinical and nonclinical data
  • Patient narratives, SAE narratives
  • Abstracts, posters, and journal articles
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Biostatistics
and data
management
Data Management
  • CRF development/validation
  • Customized database design/validation
  • Data entry screen design/validation
  • Double data entry
  • Programming under SAS
  • Data validation
  • Data listings
  • Convenient data format for the client
  • Data transfers
  • Data coding
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CTM
Logitics
CTM Logitics
  • Full Scope of Clinical Trial Logistics Services
  • Controlled access to storage areas
  • 24/7 receipt of IMP and CTM
  • Patented warehouse database program
  • General liability and property insurances
  • Compliance with ISO 9001:2015 & GDP
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PV
Support
PV Support
  • Therapeutic, technical, and operational excellence
  • Tailored and cost-effective safety solutions
  • Flexible outsourcing of safety functions
  • A team of QPPVs for registered products in EU
  • Updated country-specific regulatory requirements
  • Robust quality system
  • Pharmacovigilance consultancy
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Independent
Audits
Independent Audits
  • Clinical site GCP audits
  • Documentary Trial Master File audits
  • System Vendor Audits
  • Regulatory Inspection and Sponsor’s audit readiness check
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Rare and
Orphan
Diseases
Rare and Orphan Diseases
  • Circumventing recruitment challenges
  • Integrated expertise and support – what does this mean?
  • Active engagement with disease-specific societies and support groups
  • Effective use of referral sites

Türkiye

Instanbul office

Nisbetiye district, Gazi Guncar Street 4/2, Uygur business center, Besiktas, Istanbul 34340, Türkiye

Tel: +905 417 619 609

Türkiye Country Profile

Türkiye – a Hidden Gem in Clinical Research
Firstly, it is official – Turkey is now Türkiye. This change took place past summer when the United Nations officially recognized the new name.  With a population of over 85 million, a well developed universal healthcare system, a relatively low per capita number of clinical trials, a large pool of treatment-naive patients, Türkiye is...
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