Overview

What we can do for you:

• Rapid Trial Development – Dynamic architecture allows for reduced trial development time.

• On-Demand Form Generation – eCRFs are dynamically generated from a master database.

• 21 CFR Part 11 Compliant – Compliant with 21 CFR Part 11, ICH-GCP, and FDA's "Guidance: Computerized Systems Used in Clinical Trial."

• Real Time Validation/Data Cleaning – Data validation using customer specific edits and rules to ensure data integrity.

• Data Import/Export – Capable of SAS, CDISC, XML, ASCII files, and Excel spreadsheet formats.

• Alerts and Notifications – TrialMaster includes a very robust "alerts and messaging" system.

• Online Query Resolution – Our internal query resolution tool expedites monitor/investigator issues.

• Real Time Project Management – Sponsors, field managers and project managers can analyze and track ongoing research data.

• Thin Client Footprint/Browser Based – Manage your data from anywhere, anytime on the web.

Introducing TrialMaster

• Overview

• Benefits of EDC

• Application Features

• System Benefits

• Pricing

• Schedule a demo