Public / Direct Reporting
Global solution with simple, self-service interface enabling reporting at source via corporate & product websites with touchless processing
Improve control of your PV intake process
Standardise data across all intake routes, increase efficiencies, and accelerate safety insights
Highly scalable global PV platform
Transform the capture, management & processing of adverse event, drug safety & product quality complaint data
Enhance Patient Engagement
Provide a dynamic experience with standard data export
Increase Efficiencies
Streamline processes, automate transfer and reduce follow up
Simplify Safety Management
Reduce case processing and management effort for vendors and safety teams
Capture reports direct from source
Provide an omni-channel user experience to enable patient, caregiver, and HCP reporting via corporate & product websites
- Highly accessible dynamic digital interface
- Intuitive, guided workflow to ensure data is captured right first time
- Multi language Chatbot
- Enhance user experience through an interactive interface to guide reporting
- Integrate conversational AI
- Harness the power of conversation to provide a modern, consumer-led experience
Capture the right data, first time
Intuitive, empathy-driven interface
Simple, local language system connecting with all types of reporters supported by dynamic questioning to guide users and ensure key data is collected right first time across all intake channels.
Standardised case data
Consolidate the full process onto a single platform for all sources, with instream coding and consistency checks.
Any device, any time
Highly available cloud infrastructure with online/offline capability ensures data can be entered anywhere, at any time.
Streamline pharmacovigilance processes
Highly configurable platform that enables deployment in line with company branding, workflows and portfolio requirements.
- Automated workflows
- Auto-translation (all MedDRA languages)
- Auto-distribution & redaction
- System notifications
- Complete audit trails across vendors and systems
Seamless integrations
Seamlessly transfer data between systems to optimise the end-to-end pharmacovigilance process.
- E2B (R2/R3) transfer into safety databases
- Auto reconciliation of reports
- Integration with upstream and downstream systems
Enhanced visibility and control
Implement a centralised solution across all intake routes to increase data visibility and drive faster signal management.
- Real-time access to reports
- Enhanced KPI tracking and management
- Complete audit trail
- Data available immediately for regulatory reporting and analysis
Reportum Quickstart
Preconfigured and verified out-of-the-box platform for rapid implementation and cost-effective deployment
- Rapid Setup - Ability to deploy in weeks
- Affordable Pricing - Simple and fixed pricing structure
- Full SaaS Offering - Low ongoing management requirements
Transform Drug Safety Capture
Reportum is a fully configurable drug safety reporting solution, supporting adverse events and product quality complaint intake across all channels, languages, and reporter types
Field Force
Multi-lingual, intuitive interface with online/offline capability to facilitate quick & easy reporting of key information
Call Centre
Expert user interface and workflow, reducing time-per-report and reconciliation activities, ensuring complete data transfer to downstream systems
Affiliate
Guided collection, translation and automatic routing, including data redaction, resulting in improved data privacy and compliance
Patient Support Programs
Program specific solution for nurses or case managers enabling standardized and complete data capture across multiple third-party service providers
Risk Management / REMS
Unified solution for required training & certification of HCPs, and the capture of adverse events including targeted questionnaires
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