adWATCH
adWATCH - AE streamlines the generation and management of Adverse Event Reports (AERs) for pharmaceutical organizations amidst clinical trials. By utilizing user-friendly electronic forms, it facilitates the accurate filing of MedWatch and CIOMS reports. This efficiency enhances compliance with regulatory requirements while ensuring timely communication with relevant agencies and stakeholders.
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Top adWATCH Features
- User-friendly interface
- Standardized electronic forms
- Seamless protocol integration
- Fast AER generation
- Automated report filing
- Multi-platform availability
- Compliance with FDA regulations
- CIOMS report generation
- Medical complaint tracking
- Real-time reporting capabilities
- Customizable report templates
- Alerts for missing information
- Role-based access controls
- Comprehensive data analytics
- Audit trail functionality
- Secure cloud storage
- Integration with existing systems
- Multi-language support
- Training and support resources
- Free demo availability.
