Revolutionizing Clinical Trial Execution
With decades of clinical research experience, we aim to transform the existing clinical trial paradigm by empowering clinical trial sponsors, research centers, and contract research organizations (CROs) to shift towards a more efficient model. Our innovative approach establishes a new standard for conducting clinical research, emphasizing the maximization of productivity and efficiency at research centers
Our consulting practice is led by Prof. Igor Bondarenko, MD, a distinguished expert with 25 years of experience in conducting complex clinical studies in oncology as the Principal Investigator. Professor Bondarenko has overseen more than 520 Phase I-III studies, demonstrating unparalleled expertise and leadership in the field.
Under his guidance, the research center has achieved the highest levels of patient enrollment in over 30 studies and has been recognized as a center of clinical excellence. Over 5,000 patients have participated in clinical studies at his oncology-dedicated research center, reflecting his commitment to advancing cancer research and improving patient outcomes.
Our mission
Our mission is to improve the efficiency and quality of clinical trials at sites by developing a new paradigm for conducting research through the strategic application of management, analytical, and technological solutions.
25+ years
experience in conducting clinical trials
525
studies successfully conducted in the field of oncology
5000
patients participated in clinical studies at our oncology-dedicated clinical research center
Who do we work with?
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Clinical site management
Our expertise
- Inspection of clinical premises and development of an individual reconstruction plan
- Analysis of technical capabilities and creation of a technical update scheme
- Personnel development assessment and recommendations for training plans
- Timetable and roadmap for center development enhancement
- Site feasibility assessment and selection of centers
- Execution of clinical trial agreements
- Collaboration with ethics committees
- Patient treatment in clinical trials
- Maintenance of medical records
- End-of-treatment and follow-up phases
- Invoicing
- Study closure and archiving
Clinical trial management
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Our expertise
- Multilingual system for managing the operations of research centers within a single project
- Selection of countries and research centers
- Study budgeting and contract negotiation with sites
- Patient recruitment strategies
- Patient retention and follow-up strategies
- Monitoring
- Cultivating relationships with clinical research sites
- Developing partnerships with Key Opinion Leaders (KOLs)
- Audit and inspection readiness
- Vendor management
- Trial Master File (TMF) management
- Study result publication
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Technology
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Our expertise
- Clinical Trial and Site Management System
- Remote monitoring and data management
- Pharmacy management, accounting and storage of medicinal products
- Automated creation of medical records
- Automatic invoicing
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Mentoring
Our expertise
- One-on-one, departmental, and organizational mentoring
- Thorough study setup before study commencement
- Comprehensive strategies for managing clinical research sites
- Strong partnerships between sponsors and centers
- Strategies for financial control and motivation