Testimonials

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Working with the Centre for Vaccinology (CEVAC) has been an excellent experience. The team consistently demonstrates a high level of professionalism, scientific expertise, and a truly service-oriented approach. Their staff is knowledgeable, proactive, and always focused on finding practical solutions.

CEVAC excels in the planning and coordination of subject visits, ensuring recruitment schedules remain on track while maintaining flexibility whenever needed. Data entry into the EDC system is accurate and completed with impressive speed, contributing to efficient trial oversight. Requests are handled with a quick turnaround, and communication is always timely, transparent, and collaborative.

Beyond outstanding site operations, CEVAC provides valuable scientific and operational support throughout the entire clinical trial lifecycle. Their expertise has been instrumental in ensuring a smooth and efficient study execution. CEVAC has shown to be a highly reliable research partner that consistently delivers high-quality work, and we look forward to collaborating with them on future clinical trials.

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During the past years, we have collaborated with CEVAC on several clinical trials, and our experience has consistently been very positive. From start to finish, the entire team is highly involved and ensures that everything is carefully followed up. Their clear and structured approach, combined with open and transparent communication, enables clinical trials to run smoothly and efficiently. The quality of the source documentation is very high, and the number of protocol deviations is low. In addition, their participant retention rate throughout the entire trial is remarkable.
What we particularly appreciate is their flexibility and proactive mindset: whenever challenges arise, the CEVAC team actively thinks along with us and works together with us to find effective solutions.
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We highly valued our collaboration with the clinical site CEVAC in Ghent. Despite regulatory challenges, their flexibility and proactive approach ensured the study started as planned. The team communicated clearly, addressed issues promptly, and consistently delivered on commitments, making them a reliable and trustworthy partner for clinical trials.