We understand that the success of your biotech research hinges on insightful medical expertise and proactive monitoring, especially within the complexities of oncology and rare diseases.
At Evestia Clinical, our dedicated medical affairs and medical monitoring teams work as an integral part of your drug development process. We believe in a collaborative approach, taking the time to thoroughly understand your therapeutic goals and challenges.
Our experienced physicians and medical experts provide strategic input from early planning stages through trial execution, offering guidance on protocol design, patient safety, and scientific integrity.
You can rely on our proactive medical monitoring to ensure patient well-being and data accuracy throughout your study. We are committed to transparent communication and agile problem-solving, adapting our strategies to meet your evolving needs. Our goal is to be an expert extension of your team, providing the medical insights and rigorous oversight necessary to drive your program forward with confidence and achieve meaningful results.
Count on our pragmatic approach to deliver effective medical governance and support the successful development of your life-changing therapies.
Our range of medical services includes:
- Protocol development
- Feasibility assessment and patient pathway reviews
- Medical monitoring
- Site training and physician support services
- Medical; reviews of documents
- Medical report writing
- Clinical Safety and Pharmacovigilance
