At Evestia Clinical, we provide attentive and expert clinical monitoring services tailored to the unique needs of biotech companies.
As an agile and dynamic CRO, we prioritize personalized support and build strong, collaborative relationships with our clients. Our approach ensures you benefit from dedicated and stable clinical research teams that go the distance with your project from initiation to completion, fostering a deep understanding of your objectives and avoiding the disruption of frequent team changes.
Because we genuinely care about your success, and we’re committed to delivering on your project goals while ensuring you always feel supported and confident from day one, our experienced teams are invested in your milestones. We recognize that innovative biotechs require a partner who not only understands the science but also provides hands-on operational expertise throughout the clinical trial journey.
Our team is committed to providing proactive and responsive monitoring, ensuring the integrity of your data and the safety of your patients.
We integrate patient perspectives into our approach, particularly when reviewing subject-facing materials, to ensure a truly patient-centric trial.
Our clinical monitoring capabilities encompass:
- Comprehensive site management and support
- Rigorous adherence to regulatory guidelines and GCP
- Proactive risk management and quality oversight
- Detailed data review and timely reporting
- Effective communication and collaboration with sites and sponsors
- Customized monitoring plans to meet your specific trial requirements
- Expertise across various therapeutic areas, with a strong focus in oncology and rare diseases
