Clinical Data Management CRO

At Kaairosh we believe in providing high quality clinical data management to support your drug / medical device development needs to get your products to market as quickly as possible. We provide bespoke solutions tailored to your requirements and provide real time, faster access to data meaning faster decisions can be made to keep patients as safe as possible.

As a niche data-focused CRO, our expertise allows us to focus solely on the data of a clinical trial and enables us to develop trust with long lasting partnerships. By concentrating exclusively on data we are able to offer efficient and flexible clinical data management services, we are seen as a niche provider for smaller teams or a valuable experienced partner for larger accounts.

Kaairosh provides end to end comprehensive clinical data management services from Phase I through to post-marketing trials. Our team of global clinical data management experts are committed to upholding a standardized, process-driven approach.

Our Clinical Data Management Services include:

On-shore and off-shore Clinical Data Management Services
EDC and Paper Trial Set-Up & Management
Access to different EDC solutions
Data Management Plan (DMP) development
Data Management Project Management
CRF/eCRF design and development
CRF Annotation & Review
Database Build & Design
Data validation specifications
Edit checks Programming & Testing
Data processing through double data entry
Query Management
Medical Coding
Safety Data Management & Reconciliation
Data Export/Transfer
CDASH Compliant deliverables
Real-time data viewing and reporting

The key to a successful working relationship and part of our customer excellence approach with our clients is being flexible to their requirements. Therefore, our Lead Clinical Data Managers will work with our partner customers to define specific requirements and expectations to meet the partnership objectives.

Kaairosh has experience with USFDA and EMEA submissions of clinical trial data.