Clinical Data & Site Management
Clinical Data & Site Management
Mediclin Clinical Research provides traditional Clinical Data & Site Management solutions as well as an Electronic Data Capture (EDC) and Electronic Patient Reported Outcomes (ePRO) approach, giving flexibility in data management solutions while always maintaining high standards for data quality and timeliness.
In addition to full-service clinical research trials, Mediclin Clinical Research supports many stand-alone and functionally-based biometrics projects. Clients rely exclusively on our staff to manage all biometrics aspects from rapid data entry to final trial reports. Our experience allows us to make recommendations on the most efficient and cost-effective approach for any clinical research trial.
Our Clinical Data & Site Management team has built up extensive hands-on experience with several data management systems over the past years. Therefore, our Data Management team is able to offer our clients the right solution for their projects.
As a result and similar to all other areas of our operations, Mediclin Clinical Research is able to offer the flexibility that our clients desire and require.
Often our clients require Mediclin Clinical Research to manage all Biostatistics aspects of their projects from protocol development and sample size calculation to final study report. Our experience allows us to identify the most efficient and cost-effective approach to completing your clinical trial.
Mediclin Clinical Research is well established Clinical Data & Site Management Company. We are team of experience people who are well aware of 21 CFR, HIPAA, and ICH GCP compliance to provide clinical data management services.
Mediclin Clinical Research provides traditional clinical data management solutions as well as an Electronic Data Capture (EDC) and Electronic Patient Reported Outcomes (ePRO) approach, giving flexibility in data management solutions while always maintaining high standards for data quality and timeliness.
At Mediclin Clinical Reseach, our experts are committed to give high-quality, reliable, and statistically sound data from clinical trials in the compliance of 21CFR, HIPAA, ICH GCP. We perform prompt services of data management, CRF designing , CRF tracking, test script and UAT, data entry, data verification, query generation, discrepancy resolution, data validation specification, statistical analysis, trial reporting services in India, USA, Europe, and Australia.