GENELYTICA

GENELYTICA is a Clinical Research Organization with a global footprint and over eight years of experience offering comprehensive and specialized CRO services for pharmaceutical, biotech, and medical device companies. With wide range of experience, as well as, clinical teams across 15 countries in EU, US, and Asia, we ensure compliance with EU MDR and US FDA regulations, while streamlining your clinical trials and reducing time to market, all while keeping your costs down. We help our partners in specific trail areas or end-to-end trial management, from drafting a study protocol and its medical evaluation, preparation of required documentation, through a selection of appropriate sites, submission of the trial to competent bodies and Bioethics Committees, negotiation of contracts with the sites, supporting the patient recruitment process, monitoring and close-out visits to drafting the final study report. Why us? • Partner Focused and High Quality: We have a strong experience while focusing on a handful of project at the same time. • Excellent CRA Team: seventy percent of our associate bring oncology and medical device experience. • Experienced Recruitment and Retention Team: known for hitting and beating the site activation and enrollment goals. • Budget Friendly: With headquarters in Poland and strong operations in Eastern Europe, we are able to deliver high quality results while being budget friendly. • Safety Driven: focused on safety of all trial patients and PV reporting. • Proactive Communication: Direct, clear and quick communication, while responsive and flexible based on trial needs. • Results Driven: Meeting and exceeding our milestones and ultimate trial goals. Backed by our clinical trial guarantee. Our experience and resources include: • Countries with operations and partnerships: 15 • Clinical trials: 50+ • Indications: 30+ • Patients: 2000+ • Trial sites: 250+ Please feel free to contact us for any help in your Phase 1, 2 and 3 trials.