IRMS AE
Adverse Event Module

WHAT IS IRMS?

IRMS (Information Request Management System) is Anju’s recognized system for Medical Affairs input. Our system allows you to easily capture requests for medical information, adverse events, and product complaints and quickly respond to those requests and accurately report and track all necessary activity irrespective of what system you use for AE or Product Complaints. Our system will funnel the information based on the type of input to the right software and track that it is tracked and acted on. Anju BUS and AI based data movement, the input into Anju would provide one source of tracking ALL input for Medical Affairs group.

The IRMS-AE Capture module is designed for companies that have an existing Adverse Event system already in place. IRMS-AE allows for the capture of detailed Adverse Event data, from patient and medication information to MedDRA coding and outcome data. This information can then be transferred to the appropriate safety department or safety system either manually or automatically.

ALLOWS YOU TO CAPTURE:

  • Patient and outcome related information
  • Multiple suspect and concomitant medications
  • Multiple AE terms with all related information
  • Multiple test and lab data
  • Multiple previous medical history information
  • Detailed case activity, with dates and notes

FULL IRMS INTEGRATION

IRMS-AE is designed to fully integrate with its medical information system parent solution, IRMS. This integration allows for a single point of entry for all Pharmacovigilance, Medical Information, contact and correspondence management, and adverse event data entry. Additionally, the full IRMS-AE system allows for real-time case transfer to any existing industry standard adverse event systems.

CLOUD-BASED DEPLOYMENT OPTIONS

The IRMS-AE solution can be deployed as a cloud-based package or implemented on premise. With either solution, IRMS-AE provides for configurable security parameters which allow for partner case processing. Partners, Vendors or affiliates can utilize a single interface and repository for safety cases, eliminating duplicate data entry and the risk of conflicting case data.

USE YOUR OWN WORKFLOW PROCESS

IRMS and IRMS-AE is designed to easily configure to your own processes without customization, including unique configurations for different affiliates and partners using the same implementation. This can greatly improve efficiency and collaboration while still ensuring adherence to global and local regulations.

IRMS is the industry standard for medical information management software.

Anju has developed technology solutions that enhance the value of its core vertical products.

LEARN MORE ON THE TECHNOLOGY PAGE

Modules that extend base IRMS functionality and allow you to customize for your requirements:

IRMS-QA

Quality Assurance Module

IRMS-QA provides a powerful yet easy-to-use tool for reviewing IRMS cases or other data and reporting on the results of those reviews.

More about IRMS QA

IRMS-AE

Adverse Event Module

IRMS-AE allows for the capture of detailed Adverse Event data, from patient and medication information to MedDRA coding and outcome data.

More about IRMS AE

IRMS-PC

Product Complaint Module

IRMS-PC can handle all your product complaint tracking and correspondence data seamlessly from within a case or simply capture the required information.

More about IRMS PC

IRMS-CM

Content Management Module

IRMS-CM is a web-based solution that allows multiple departments to generate , review and manage MI materials.

More about IRMS CM

IRMS CARE

Self-Service Portal

HCP’s and consumers search for published content that has been approved by the client.

More about IRMS Care

How can IRMS help your business?