Precision for Powerful Outcomes
From CRF design to database validation, our Data Management team ensures that your clinical trial data is captured, validated, and consolidated with precision. With rigorous quality control at every stage, we support accurate data collection and compliance, setting a strong foundation for analysis and regulatory submission.
01.
CRF Design & Development
Our custom-designed Case Report Forms (CRFs) capture relevant data points accurately and efficiently, tailored to your study’s specific requirements.
02.
Database Design & Validation
We develop secure, compliant databases optimized for data accuracy and easy access, supporting the study from data collection through final analysis.
03.
Query Generation & Resolution
To maintain data consistency, our team proactively generates and resolves queries, ensuring that data discrepancies are promptly addressed.
04.
Medication Dictionary Coding
Standardized medication coding streamlines data categorization, supporting accuracy across datasets.
05.
SAE Reconciliation & Discrepancy Management
We prioritize rigorous reconciliation to manage Serious Adverse Events (SAEs) and resolve discrepancies for consistent safety reporting.
06.
Quality Control (QC)
Our data management includes ongoing QC checkpoints to ensure data accuracy, from collection to final database lock.
07.
Data Consolidation & Conversion
We handle data consolidation and conversion to integrate and prepare your data for analysis, supporting a smooth transition to the biostatistics phase.
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