Clinical trials core facility
A Clinical Trials Core Facility (CTCF) of the IMTM is a centralized unit devoted to supporting the entire lifecycle of clinical trials. From design and management to execution, the CTCF ensures that trials are conducted efficiently, ethically, and in adherence to all pertinent regulations. Our aim is to prioritize patient safety, uphold data integrity, and achieve robust scientific outcomes. Our CTCF boasts designated consultation spaces and cutting-edge ISO 15789 and ISO 17025 certified clinical laboratories. Our top-tier electronic data systems (ClinData and ClinLab) guarantee efficient data management, while our specialized cold storage within the IMTM biobank caters to materials with precise temperature requirements. The list of ongoing or closed clinical trials is listed here. By offering this suite of comprehensive services, we position ourselves as a leader in the clinical research landscape, dedicated to advancing the field for the betterment of healthcare and patient welfare.
Why Choose Us:
- Experience and Expertise: With years of industry knowledge, our team comprises some of the brightest minds in clinical research.
- Cutting-Edge Technology: We invest in the latest tools and technologies to deliver efficient, precise, and reliable results.
- End-to-End Solutions: We're a one-stop solution, managing all aspects of clinical trials, freeing researchers to focus on outcomes.
Streamlining clinical trials, we manage everything from trial registration and budgeting to contract negotiations, ensuring accurate and current trial-related documentation.
Using advanced Electronic Data Capture (EDC), we emphasize data accuracy through stringent validation processes. Our secure storage ensures data safety and accessibility for reporting.
We deftly navigate regulatory intricacies, managing submissions to health authorities, and cultivating strong relationships with ethics committees. We're always inspection-ready, meeting and exceeding standards.
Researchers can tap into our deep expertise for trial design consultation and precise endpoint definition. We also conduct feasibility studies, assessing trial practicality and operational prospects.
From screening to enrollment and follow-up, our patient-first approach ensures a smooth and informed journey for all participants.
With a keen eye on data quality and protocol adherence, our regular site visits and rigorous checks ensure the integrity of every trial.
Patient safety is paramount. We meticulously monitor adverse events, perform in-depth safety data analysis, and promptly report findings to appropriate authorities
Our team provides invaluable guidance on effective statistical methodologies, from sample size calculations to intricate data interpretation.
Recognizing the evolving nature of clinical research, we offer regular training on Good Clinical Practice standards, ethics, and operational procedures.
At the nexus of academia and industry, we foster meaningful collaborations, driving clinical research innovation and progress.
If you have any questions or would like to discuss your clinical research needs, please don't hesitate to reach out to us. Our friendly and knowledgeable team is ready to assist you. You can contact us through the following methods:
- Phone: +420 585 632 050
- Email: email@example.com
- Location: Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry and Czech Advanced Technology and Research Institute, Palacky University, Hnevotinska 5, 779 00 Olomouc, Czech Republic
We are excited to be a part of your clinical research journey and look forward to collaborating with you on groundbreaking discoveries that will shape the future of science and medicine.