As an investigator or (academic) institution, your research needs to be innovative and cost effective. Viable research strategies need to be implemented to realize the quintessential investigator-initiated studies that are of paramount importance to gain a better understanding of disease and to develop better prevention and treatment options.
ITREAS, an organization with a strong academic footprint, enables you to design and execute your research according to industry standards, ensuring compliance with all applicable rules and regulations, reinforcing your clinical evidence.
We help you transform your science and concepts into robust clinical trials and deal with the burden of administrative and management processes.
We help you secure funding from the (bio)pharmaceutical industry and we can also function as an SME when applying for research grants from the European Union or NIH.
We offer you the following the services:
- Preparation of a ready-to-submit protocol
- Biostatistics
- eCRF development
- Feasibility assessment and selection of an adequate number of high quality clinical centres with a proven track record
- Regulatory and ethics committee submissions
- Site training
- Blinded adjudication and processing of endpoints and core safety data
- Medical Monitoring
- 24/7 Medical investigator support
- Safety Board
- Assistance with the analysis and publication strategy of the results