Clinexa offers customized Data Management solutions to our clients that best fit the needs of the clinical trial and the sponsor. Our processes are highly compliant to regulatory and international clinical trials guidelines and regulations but at the same time they are highly flexible so solutions can be individualized for each client. Our highly experienced Data Management team is continuously trained and upskilled to meet the continually changing requirements for managing clinical trial data. Following are the key services we offer:

– APAC in-region support for Data Management
– Dedicated Data Manager and support staff for each clinical trial
– Thorough Data Management Plan (DMP) and Data Validation Pan (DVP)
– Electronic Data Capture (EDC) and Electronic Case Report Form (eCRF)
– Database build and simulation
– Paper CRFs when needed
– ePRO solutions
– Medical Coding
– Edit checks and Data cleaning
– Blind review
– Database lock