With headquarters in Amsterdam and Rotterdam, CR2O has built extensive experience managing and implementing phase I-IV clinical trials in over 30 countries and accumulated expertise through >400 studies over the last decade. We also have access to Ph-I units in Rotterdam and Nijmegen, where we are conducting our early stage work.
Our therapeutic focus is oncology, vaccines, cancer immunotherapy, immunology, and autoimmune disorders. Through our network with several leading clinics and research centers in Europe we gain access to world-class scientific expertise and subject populations.
Our experience and expertise includes scientific advice planning, clinical development consulting, feasibility studies, and the entire management of clinical trials, including data management, biostatistics, pharmacovigilance, quality management, medical writing. We could also support you with IMP handling and Central Laboratory management.
Our unique combination of scientific expertise, operational efficiency and access to subjects make us an attractive partner for pharma, biotech and public organizations.
To our customers, we are ‘the right size’ full service CRO. Our experience will save you valuable time and budget, allowing you to focus on what you do best.
- Organizing and managing clinical studies
- Clinical monitoring
- Quality management
- Biostatistics and data management
- Medical writing
- Cancer immunotherapy
- Meet our Probiotics team