What Will Our Free-of-Charge Feasibility Report Include?
Study Design Advice
Trial Objectives Review
Geographic Coverage Analysis
Site Selection & Assessment
Patient Recruitment Strategies
Patient Retention Plan
Regulatory Considerations
Timeline & Milestones Review
Feasibility Session Advantages
Free Feasibility Report
Receive a comprehensive Feasibility Report, packed with key findings, actionable recommendations, and strategies to maximize your trial’s performance. Use this data to make informed decisions that drive success while mitigating risks and ensuring long-term outcomes.
Increased Efficiency
Our team will help you identify and select the most suitable clinical trial sites, ensuring optimal patient recruitment and operational efficiency. With our expert planning and resource alignment, you’ll experience reduced delays and a smoother, faster trial process.
Expert Insights
Gain direct access to our seasoned industry leaders who will work closely with you to provide guidance for your specific clinical needs. From trial design to execution, we ensure that every step is optimized for success, addressing potential challenges before they arise.
Meet The Experts
Igor Bogdanoski – Feasibility Manager
- 10 years of experience in the clinical trials industry
- Member of the Association of Good Clinical Practice and Clinical Research Development
- Leads the strategic selection and evaluation of clinical trial sites, ensuring they meet operational and patient recruitment requirements
- Analyzes site capabilities, collaborates with stakeholders, and develops data-driven strategies to optimize trial success while mitigating risks, aligning resources, and ensuring efficient execution across regions
Hrabrina Hristova – Global Head of Regulatory
- Over 15 years of combined experience in the pharmaceutical and clinical research industries
- Leads the Regulatory and Safety teams at Comac Medical, providing strategic regulatory direction and developing departmental strategies
- Designs tactical development plans, conducts risk assessments, and manages critical regulatory issues to ensure compliance
- Collaborates with cross-functional teams, including project management and business development, to align regulatory goals with broader company objectives
Monica Stanescu, MD – Medical Monitor Team Lead
- 16 years of experience in the clinical trials industry, with 4 years dedicated to Medical Monitoring
- Contributed to building a dedicated Medical Monitors Team at Comac Medical
- Oversees the medical aspects of clinical trials, ensuring successful completion from a medical perspective
- Performs medical review of clinical study data and evaluates subject eligibility, analyzes clinical and safety endpoints, and provides medical insights into study designs and protocols
- Additionally, Monica supports project teams with medical guidance to optimize trial outcomes and address specific challenges
Book a Free Clinical Trial Feasibility Session
Schedule your complimentary Feasibility Session today and receive a comprehensive Feasibility Report at no cost! Our team of experts is dedicated to providing you with the insights you need to make informed decisions for your clinical trials. Our detailed Feasibility Report will include:
- Study Objectives & Design – An analysis of your trial objectives and proposed design to ensure alignment with regulatory standards.
- Geographic Coverage – An assessment of optimal regions based on patient availability, site accessibility, and regulatory requirements to enhance trial efficiency and reach.
- Site Selection & Assessment – Recommendations on the most suitable sites based on your specific needs, including site capabilities and experience.
- Patient Recruitment Strategies – Tailored strategies to optimize patient recruitment and retention, enhancing study feasibility.
- Regulatory Considerations – Insights into necessary regulatory approvals and timelines to expedite the process.
- Timeline & Milestones – A realistic timeline with key milestones for your study, ensuring efficient project management.