Clinical Research Data Management
- Data Lifecycle Management (DLM) in clinical trials covers the process from data sourcing to analytics, including clinical trial data management and clinical support services
- Data Sourcing, comprehensibility check & cleaning from various sites
- Capturing patient meta data, site data, baseline measures, dressing procedures, usage of medications, type & dimensions of wound, improvements over visits
- Analytics & Insights on medication efficacy, Usage, Site productivity
- Timely completion of Medical Records with concurrent reviews of charts and duly completing prudent PQP by our coding-billing team.
- Quality Data Submission Mandates - In the ACO environment of P4P and Value Based Purchasing (VBP) Programs, Quality Data Submissions under EHR-MU (Modified Stage-2), IQR and OQR are obligatory, facilitated by clinical support services
- Clinical trial data management using risk-based quality management is essential for ensuring data reliability. Our support services cover the entire lifecycle, ensuring compliance with regulatory requirements
For an international Wound Care Medical Tech Company focused clinical trial data management.
For Consumer Health segment of information service company.
1Mn+
Records Managed
Clinical Research Data Management
- CRF & Visits data sourcing
- Data Comprehensibility check
- Data cleaning
- Master sheet creation
- Capturing patient meta data, site data baseline measures, dressing procedures, usage of medications, type & dimensions of wound, improvements over visits
- Capturing wound images
- Patient profile over trial
- Computing site productivity
- Computing time to heal, visits to heal, degree of healing,
cost of healing
- Clinical/Operational Analytics
- Clinical support services
- Efficacy Measures
- Cost Economics
- Marketing Insights