What We Do?
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CDAQI research provides services ensuring high quality, compliant data management statistics and medical writing support to all our clients
A well designed clinical trial is complete only when backed with a good statistical analysis. Statistical analysis is critical is interpretation and applying the findings of clinical research.
When you partner with us, you are ensured of a collaboration which consists of highly qualified clinical professionals, well trained data management and biostatistics professionals who will be involved from study planning to delivery of the final report. We understand the nuances of clinical research in medical devices. In all our collaborations, we ensure our partners are involved in every stage to support their product development and certification goals. We work closely aligning the interest of our clients to that of our clinical study team to assure data is collected, managed, and analyzed efficiently. We value the data generated and its impact on improving patient care.
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Our medical writes will finally create the study reports
We are pleased to provide you with the following services
- Protocol development
- Electronic case report form (eCRF) design
- Patient enrollment, registration and site activation
- Electronic patient reported outcomes collection and analysis
- Statistical Analysis plan
- Outcome relevant high quality biostatistics
- Medical writing

Biostatistics Support
