YOUR FIRST CHOICE FOR QUALITY,
COST-EFFECTIVE GLOBAL DATA MANAGEMENT SUPPORT
Timely receipt of accurate clinical data is a necessity. BMA has over 15 years of experience in Data Management.
Accurate and complete data for submission to regulatory agencies around the world is critical for clinical studies. Our staff will work with your investigative sites, field monitors, and the study team to promptly collect and review data for precision throughout the life cycle of your trial.
"Get the most out of your study and resources by partnering with BMA"
Our goal is to provide world class support services that keep your projects on time, within budget and compliant to all regulatory authorities.
- Rapid Data & Query Turnaround
- Paper & eCRF Expertise
- Global Support Capabilities
- Deadline & Rescue Support
- Data Discrepancy/Query, Dissemination, Collection & Review
- Data Form Collection & Review
- eCRF User Support & Site Training
- Laboratory Normal Range Collection, Transcription & Reconciliation
- Sponsor & Site Data Entry
- Patient Tracking & Post-Study Follow-Up
- Clinical Scientist Support
- Patient Profile Review
- SAE & Narrative Review & Reconciliation
- Data Point Review
- Query Generation
- FDA Submission Support
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