Clinical Trial Management Software Features

21 CFR Part 11 Compliance

Shows that electronic documents are authentic and linked to specific records

Data Import/Export

Import and export information and reports to and from the program

Document Management

Collect, upload, store, and share all documents in a centralized location making it easier for everyone involved to access information

Double Data Entry

Data entry quality control method employed when data is recorded.

Electronic Data Capture

Import, collect, and capture data from multiple sources

EMR/EHR

Create and securely store patient records

Financial Management

Provide a comprehensive overview of organization's finances

HIPAA Compliant

Compliant with HIPAA, which sets standards for sensitive patient data protection

Inventory Management

Track and manage the quantity of resources on hand to maintain proper supply

Patient Management

Patient tracking throughout the facility, be it a hospital or a smaller healthcare clinic, and patient queue management.

Patient Monitoring

Observation and tracking of a patient's conditions over time

Patient Recruiting

Helps clinical trials/labs get patients for participation.

Randomization

Randomize the displayed order of questions and answer options

Scheduling

Plan availability and assign specific time slots for tasks and resources

Trial Design

Allows clinics and academic institutions to create trials and studies from scratch.

Workflow Management

Create, design, and visually represent processes within the software

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