CLINICAL TRIAL DELIVERY
Empowering Better Clinical Trial Delivery
Combining Clinical Operations, Interactive Response Technology (IRT), and Safety & Pharmacovigilance capabilities, we help sponsors streamline workflows, improve visibility, enhance data quality, and drive efficient study execution from startup through closeout.
DATA MANAGEMENT SERVICES
Full lifecycle support, start-up through archival
From study start-up to database lock, our data managers ensure clean, complete, and actionable data that keeps your trial on track and supports confident decision-making.
Start-Up & Planning
- Protocol Review
- Optimal Technology Solution Recommendation
- Risk-Based Monitoring Strategies
- Data Management Plan Development
- Data Validation Manual Development
Build & Setup
- CRF Design and Development
- CRF Completion Guidelines (CCG) Development
- Subject Diary Design and Development
- Clinical Database Creation, Validation and Auditing
- Edit Check Programming, Validation, and Testing
Conduct & Support
- 24/7 EDC Helpdesk
- EDC Access Administration
- EDC System Training for Sites and Monitors
- Data Management Trial Master File Set-Up and Maintenance
- Development of Custom Status Reports
Cleaning & Coding
- Continuous Data Cleaning Throughout Study
- Import, Integration, and Cleaning of Electronic Data
- Adverse Event, Concomitant Medication, and Medical History Coding
- Query Reconciliation
Need an EDC right away?
Clinical timelines don’t wait—and neither should you.
When a client recently faced an aggressive timeline, we partnered closely to deliver a full MedNet EDC build in just 6 weeks—providing a compliant, fully configured system that kept their study moving forward without compromise.
Get to Know More
EDC Technologies
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Data Management Rescue
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EDC Build Bottlenecks Slowing Study Startup - Blog
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EMPOWER YOUR CLINICAL DECISIONS
Let's talk about your data management needs
Connect with our data management team to scope your study's CRF design, EDC support, and closeout plan.
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