Compier IRT with Mailbox

Home / Innovation / Compier IRT with Mailbox

Establish an automated AE Intake, Receipt and Triage Capability using Artificial Intelligence

Compier IRT with Mailbox

Compier IRT enables Pharma companies to simplify multi-channel adverse event case intake, receipt, and triaging. The advanced automation capabilities facilitate fast and intelligent case intake from various channels in different data formats. It also has a built-in Inbox for distribution of emails on safety mailbox to different business partners and vendors.

Key Product Features

With a robust multi-channel case intake capability, collect all inbound cases from various channels including web, email, clinical trial portals, mobile app, etc. Cases from social media, literature and HCPs can also be redirected for receipt and triage.

Leverage ready to be deployed automation capabilities through OCR and Artificial Intelligence using NLP/ ML techniques to automatically parse raw source data and create a structured AE case from standard form such as CIOMS or and nonstandard AE Report/Snapshot.

Using the built-in email Inbox, all incoming adverse event cases from multiple stakeholders and sources can be centrally managed without having to use any other external email system. A case can be created directly from inbox with the source attachments after which receipt and triage workflows can be triggered.

Keep a track of all inbound case status and avoid delays in adverse events case processing with automatic process alerts and notifications. Reduce process deviations, quality deficiencies and eliminate compliance shortfall with immediate time-bound email alerts.

All received AEs and their versions can be triaged automatically to downstream drug safety systems using industry data standards such as E2B R2/R3 formats. Industries most used safety databases such as Oracle Argus Safety, Aris Global Lifesphere are seamlessly supported with our Bi-Directional integration.

Compier IRT is available on iOS and Android devices with support of data capture on configurable forms. Solution can also be deployed as a web portal for submission of Adverse Events for intake, review and further processing.

Get insights into operational and intake data with our built-in reporting and analytics module. Our Solution comes with 40 + standard reports and dashboards.

Compier IRT adheres to global compliance such as GxP, HIPAA and EU-GDPR regulations with the setup of country specific data privacy rules. Organization can conduct business operations as per applicable data protection company policies.

Compier IRT is a 21 CFR Part 11 and Annex 11 Compliant solution with a non-editable audit trail and transaction history for all the activities performed in the system.

Technology Image

Solution Benefits for Clients

  • Improve Efficiency and Productivity
  • Improve Adverse Event Data Quality
  • Structure the Unstructured Data with AI
  • Achieve Speed with Automation and Integrations
  • Achieve Global Regulatory Compliance
  • Address Current and Future Business Needs
  • Lower Total Cost of Ownership

How Do we Deliver

Compier IRT with Mailbox is a component of our Compier platform. It can be deployed on its own or in combination with other modules of the platform such as Case Exchange & Reconciliation, L2A Filter etc.

Latest News / Articles

Food & Nutraceuticals: How Companies can Prove Health Value with Clinical Trials

What are Food and Nutraceuticals? ‘Nutraceuticals’ is a composite term of ‘nutrition’ and ‘pharmaceutical’. They are a blend of products that possess both nutritional as well as medicinal value. They are designed to improve physical health, boost immunity, and deal with stress and increase longevity. Nutraceutical products play a significant role in maintaining normal physiological [...]

Best Practices for Signal Management in Pharmacovigilance

Pharmacovigilance involves the collection, detection, assessment, and monitoring of data on Adverse Drug Reactions (ADRs) which must be evaluated to derive vital safety information. Signal detection involves monitoring the adverse reaction data for patterns that suggest new safety information. Safety signals can be detected from an extensive range of sources, such as spontaneous reports, clinical [...]

Enabling eSource in Clinical Studies to Optimize Trial Quality

Source data is all information in original records and certified copies of original records of clinical findings, observations, or other activities in a clinical trial necessary for the reconstruction and evaluation of the trial. The electronic data source or eSource is the data that is initially recorded in electronic format in this process. Biopharma and [...]

Get in Touch with Us