Multisource Inbox

Need for this

Adverse event (AE) reports come from multiple sources - healthcare professionals, patients, literature reviews, internal quality teams, and regulatory agencies. Managing all this data from different channels can be overwhelming, leading to missed safety signals, delays in case processing, and compliance risks. A centralized system is essential to collect, manage, and prioritize these reports efficiently, ensuring nothing falls through the cracks and every case is handled promptly. 

How it Benefits

Centralized Data Collection

Aggregates case data from multiple sources into a single platform, eliminating scattered information.

Efficient Triage and Prioritization

Helps identify critical cases quickly, ensuring urgent reports get immediate attention.

Improved Signal Detection

Provides a structured approach to identifying potential safety risks early.

Regulatory Compliance

Ensures all AE reports are managed according to industry standards and submission timelines.

Reduced Data Redundancy

Prevents duplicate entries and optimizes case processing efficiency.


How We Are Using This in Existing Products

In PvEdge®, the Multisource Inbox is designed to seamlessly gather and organize AE reports from various channels. The system automatically sorts and categorizes data, enabling faster review and decision-making. By integrating with other PvEdge® modules, it supports a smooth workflow from intake to final submission, ensuring that pharmacovigilance teams can efficiently manage case volumes without missing critical safety insights. 

Result of Implementation of PADER

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Time Savings

Reduced manual effort in collecting and sorting reports.

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Higher Accuracy

Improved data consistency and minimized duplication.

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Enhanced Compliance

Streamlined reporting aligned with regulatory requirements.

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Scalability

Ability to handle increasing AE report volumes without workflow disruptions.

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