Provide an intuitive and engaging reporting experience that works on users’ preferred devices and in their local language.
Achieve global consistency with a single, centralized, and fully audit-trailed solution for all intake routes and follow up.
Streamline pharmacovigilance processes by digitizing intake, output, and eliminating manual steps.
Unified capture of data through a single workflow engine enabling digital intake at source or automatic import of structured forms across languages.
Tailored experience based on user type, product, and nature of adverse events.
Eliminate manual reconciliation through automated E2BR2/R3 transfer into the safety database.
High availability and high-performance cloud infrastructure to manage rapid shifts in adverse event reporting.
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.
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.
2 Leman Street,
London, E1W 9US
United Kingdom
Company number: 13916274