Our expertise spans every stage of clinical research, including trial conceptualization, operational implementation, statistical analysis, data management, and quality assurance.
Leveraging the extensive scientific and clinical expertise of our faculty, global academic networks, and a highly skilled team, we are committed to achieving excellence in clinical trial management. From designing and executing studies to disseminating results, our goal is to enhance the impact of clinical research on health.
Our Mission and Vision
The MedIC CTU will play a crucial role in fostering a dynamic and responsive research environment that spans the full spectrum of medical research—from bench to bedside. By facilitating collaborative efforts with academic institutions, enterprises, and industry, we aim to create a research ecosystem that thrives on innovation and excellence.
Key Focus Areas
The EUC MedIC CTU will manage a diverse portfolio of trials, including early to late-phase studies, with an emphasis on MedIC Core areas, including:
- Infectious Diseases, Microbiology and One Health
- Cardiorespiratory Medicine
- Hematology/Oncology
- Neuroscience
Our focus will include biomarker-driven and innovative trial designs to ensure impactful outcomes.
Our Core Functions
The MedIC CTU will provide comprehensive support throughout the lifecycle of clinical trials, including:
- Design, Conduct, Analysis, and Reporting: Ensuring robust management of clinical trials from start to finish.
- Evaluation and Documentation: Systematic review and documentation of clinical trial applications.
- Quality and Safety: Upholding the highest standards of quality, safety, and ethical conduct.
- Adverse Events Monitoring: Collection and analysis of data on adverse events during trials.
- Regulatory Compliance: Adherence to Good Clinical Practice (GCP) guidelines and EU regulations.
- Training and Development: Providing educational opportunities and training for research personnel.
Collaborative Approach
By partnering with local enterprises and international experts, the MedIC CTU will address shared challenges, exchange best practices, and establish common approaches to clinical research. Our coordinated strategy will include attracting industry collaborations and developing mandatory guidelines, accreditations, and agreements.
Building the Future
Our commitment to integrating clinical research with healthcare needs aims to shape the clinical trials workforce of tomorrow. The MedIC CTU will attract top-tier research staff, offer training initiatives for investigators, statisticians, and unit members, and embed scientific expertise in trial development.
As a Centre of Excellence within European University Cyprus, the MedIC CTU is aligned with the institution’s mission to promote education and research, influence policy, engage in competitive funding, and enhance its presence in the clinical research community.
We look forward to driving progress in clinical research and making a significant impact on patient care through our innovative and comprehensive approach.
Large-Scale Trials
At MedIC CTU, we employ an agile service model that integrates scientific, clinical, and operational expertise. By closely collaborating with sponsors, we plan and conduct large-scale national and international clinical trials, guiding them from inception to completion. Our team proactively addresses challenges in implementation, accelerating progress for our partners and amplifying the impact of clinical innovations.
We prioritize building long-term strategic alliances with industry and academic partners, working together to generate significant health benefits for patients worldwide.
Comprehensive Clinical Research Services
Our team’s expertise covers a wide spectrum of clinical research activities, including:
- Designing studies with multi-disciplinary teams
- Conducting literature reviews and writing protocols
- Developing and managing databases for multi-phase studies and trials
We also offer specialized services such as:
- Ethics and regulatory submissions
- Conducting site feasibility assessments and setups
- Developing risk assessments and monitoring plans
- Implementing risk-based monitoring strategies
- Overseeing trial close-out and database lock procedures
- Preparing peer-reviewed academic journal papers and presentations for public dissemination
CTU Committee
CTU Lead: Christina Kousparou
- Dr. Aris Angouridis
- Dr. Andreas Larentzakis
- Dr. Constantinos Tsioutis
- Dr. Theodore Lytras
- Dr. George Georgiou
- Dr. Constantinos Zamboglou
For more information about our research staff, services, and collaboration opportunities, please contact our team.