GeoStorage
УслугиО насПартнерыKnowledge HubКонтакты
Guides & Best Practices

Доступ пациентов и набор участников — расширение доступа к группам пациентов, ранее не получавших лечения, и увеличение плотности исследовательских центров

GeoStorage
15 сентября 2026 г.
3 мин чтение
Поделиться:
Доступ пациентов и набор участников — расширение доступа к группам пациентов, ранее не получавших лечения, и увеличение плотности исследовательских центров
 
Executive Overview 

Achieving 6-8 week trial activation timelines means little if patient recruitment cannot keep the enrollment schedule. Enrollment delays remain the single largest cause of protocol amendments and trial extension costs globally, with up to 80% of clinical trials failing to meet their initial enrollment deadlines. 

Georgia addresses this bottleneck through two primary structural advantages: high concentrations of treatment-naive patient cohorts and dense, high-volume clinical site networks. By leveraging centralized medical hubs, high patient-to-site ratios, and strong investigator-patient trust, sponsors routinely achieve accelerated recruitment rates across complex therapeutic areas. 

Global Benchmark Enrollment:  [====== Slow / Fragmented ======] ➔ High Dropout Rates 

Georgia Recruitment Model:   [== Dense Hubs ==] ➔ Rapid Accrual ➔ Superior Retention 

1. High-Density Medical Hubs & Concentrated Pools 


Unlike geographically dispersed trial networks that require dozens of low-enrolling sites, Georgia’s healthcare infrastructure is highly centralized around key metropolitan hubs: Tbilisi, Kutaisi, and Batumi.

Georgia's clinical research hubs: Tbilisi, Kutaisi and Batumi

 
Centralized Patient Flow: Over 70% of specialized medical care and trial activity is concentrated within major medical centers in Tbilisi, allowing single sites to draw from large catchment populations. 

  • Streamlined Site Selection: Sponsors can achieve target recruitment goals using fewer overall sites, reducing site management overhead, monitoring costs, and administrative burdens.

 

2. Treatment-Naive Cohorts & Therapeutic Density 


Georgia provides exceptional access to diverse, well-defined patient populations across key indication areas where trial competition in Western Europe and North America creates severe recruitment friction. 

  • Oncology & Hematology: Rapid access to treatment-naive patients across solid tumors and hematological malignancies, facilitating clean baseline data collection for early-to-late phase oncology protocols.
  • Infectious Diseases & Immunology: Strong patient volume in respiratory, viral, and autoimmune conditions, supported by specialized tertiary referral centers.
  • Cardiology & Metabolic Disorders: High prevalence of cardiovascular disease, diabetes, and metabolic syndrome, enabling rapid accrual for large-scale outcomes trials.
  • Neurology & Rare Diseases: High referral compliance through centralized specialist networks, ensuring high screen-to-randomization ratios.

3. High Patient Retention & Protocol Adherence

 
Recruitment is only half the battle - retaining trial participants throughout the study lifecycle is essential for data integrity and power calculations.
 
Patient retention enablers in Georgia

 
  • Physician-Patient Relationship: Clinical trial participation in Georgia is strongly driven by investigator recommendation, yielding low drop-out rates and high visit compliance.
  • Operational Continuity via GeoStorage: Local depot availability ensures that clinical supplies, diagnostic kits, and temperature-sensitive IMPs are never stock-out delayed. Optional Direct-to-Patient (DTP) home delivery protocols keep home-bound or distant patients fully engaged without missed doses.

Summary of Patient Access Advantages

Metric / ParameterGlobal StandardGeorgia NetworkStrategic Impact
Sites Needed per ProtocolHigh (10–20+ sites)Consolidated (3–6 sites)Lower monitoring costs and site overhead
Treatment-Naive PoolHighly Competitive / SaturatedAbundant Across Core IndicationsFaster enrollment & clean baseline data
Patient Retention Rates70% – 85%90%+Minimized drop-outs & robust protocol data
Supply ContinuityFragmented Cross-BorderLocal GeoStorage Depot & DTPUnbroken drug delivery to trial participants


GeoStorage

Excellence in medical research and clinical trial management since 2010.

Company

  • About Us
  • Our Team
  • Knowledge Hub
  • Contact

Legal

  • Privacy Policy
  • Terms of Service
  • Certifications
  • Compliance
LinkedIn

© 2025 GeoStorage. All rights reserved.

Contact Us