Provide an intuitive and engaging reporting experience that works on users’ preferred devices and in their local language.
Control Pharmacovigilance Workflow
Achieve global consistency with a single, centralized, and fully audit-trailed solution for all intake routes and follow up.
Reduce Effort and Costs
Streamline pharmacovigilance processes by digitizing intake, output, and eliminating manual steps.
Fully Verified and Highly Scalable SaaS Platform
Digital and Pharmacovigilance Forms Intake
Unified capture of data through a single workflow engine enabling digital intake at source or automatic import of structured forms across languages.
Configurable Platform
Tailored experience based on user type, product, and nature of adverse events.
Seamless Integration
Eliminate manual reconciliation through automated E2BR2/R3 transfer into the safety database.
Scalable and Secure
High availability and high-performance cloud infrastructure to manage rapid shifts in adverse event reporting.
Reportum® PV Design Studio
Configurable Forms for Seamless Data Capture
Using our PV Design Studio, Reportum® offers configurable forms tailored to your business needs, including your portfolio, therapy areas, and geographies, ensuring seamless alignment with your workflows. Our platform allows you to capture data from all sources with precision. With our deep pharmacovigilance expertise, Qinecsa ensures accurate data capture, delivering it directly to your safety database.
Adverse Events (AE) & Product Complaints (PC)
Patient Support Programs, Market Research, Call Centers
Capture data from all sources with configurable workflows
Extensive data capture for E2B or custom fields with seemless ingegrations to downstream systems
Intelligent search and library support (MedDRA, UCUM, Product Library)
Multilanguage support for global scale
White labeling
Expert Guidance & Support
Our experts guide you from initial consultation to final deployment, ensuring compliance and usability. We will ensure the forms efficiently capture all necessary data while staying compliant with regulatory standards.