
"From the research lab directly into clinical research. For over a decade, I've been on a mission for you to create efficient project solutions and synergies for innovative research."
[Founder Kim-Maria Eilitz]
We are not a CRO, but your smart pilot to project success. We develop customized solutions for your clinical trial.
The REA experts will support you with the following essential questions and more:
- Feasiblity / Study Start Up
- Regulatory planning
- Investigational Sites
- Patient recruitment
- Monitoring
- Clinical Study Report
- Approval
- Follow Up Planning
- Post-market concepts
Our experts all have many years of expertise in the field of medical device technology and pharmaceutical products and beyond. We work exclusively according to the latest national/international guidelines and standards*.
*For example: Medical Device Regulation, AMG, ICH/GCP, ISO14155
"Whether as a business angel, coach or interim manager, as a mentor and expert I support projects in different settings. With REA, I create customized solutions in a flexible and agile work environment. Always in focus: research and business goals!"
[Founder Kim-Maria Eilitz]
Together with you, an experienced team of experts develops suitable solutions for your clinical study. According to the individual study phases (Phase I- IV), the planning and concept development takes place in accordance with the requirement areas. We accompany you for maximum project success and develop optimal processes for your clinical study.