About Us

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OUR VISION

We are committed to contributing to the advancement of medical and pharmaceutical research in Armenia, striving to improve human health through every study we undertake.

OUR MISSION

Through steadfast commitment to quality and excellence, we aim to establish Armenian medical centers as the preferred destinations for clinical trials.

OUR PRINCIPLES

Our business model accelerates the start-up phase, ensures effective patient recruitment, and delivers accurate, timely data. We guarantee efficient completion of trials and reliable data from every patient involved in the clinical trials we support

Our Advantages

  • Precise identification of customer needs with tailored, high-quality services and solutions
  • Extensive expertise in project management across all trial phases
  • Partnerships with the largest university hospitals, providing access to a diverse patient population with various medical conditions
  • Streamlined processes through an advanced CTMS system, ensuring consistent high quality and operational standardization
  • Comprehensive SOPs, training programs, and a robust quality assurance system
  • A highly skilled, well-trained team of medical professionals
Advantages
Benefits

Benefits For Sponsors and CROs

  • Access to an extensive network of investigators and referral physicians for multi-centric clinical trials across diverse therapeutic areas
  • Investigators are Key Opinion Leaders (KOLs) with access to extensive databases covering a substantial part of Armenia, providing a vast pool of patients and ensuring comprehensive recruitment capabilities, even for rare indications
  • Direct access to rare conditions and naïve patient populations
  • Free, comprehensive, and fast project feasibility assessments
  • Efficient procurement and preparation of regulatory and feasibility documents
  • Single point of contact for streamlined budget negotiations and contract management
  • Support for patient enrollment at all stages of the trial
  • Full administration and management of clinical trials within dedicated research centers
  • Locally positioned experienced site research coordinators embedded in study teams
  • Study-specific eSOURCE for remote monitoring, saving time, costs, and resources

Benefits For Investigators and Institutions

  • Reduce investigator workload by 70-80%, allowing focus on medical activities while we handle logistics and administration
  • Full preparedness for inspections at any time
  • Dedicated site research coordinators act as liaisons between sites, CROs, and sponsors
  • Elevate the scientific profile of hospitals and investigators
  • Increased opportunities for scientific publications and international collaboration
  • Access to more patients through referral networks and our extensive database
  • Generate additional income by attracting new studies, increasing subject enrollment, and improving retention
  • Study-specific eSOURCE development for high-quality data, improved compliance, and time-saving remote monitoring
  • Regular study reports on timelines, enrollment, and financial data for greater clarity and motivation
Investigators