Neovero Vigilance
An integrated technovigilance module for reporting, investigating, and tracking incidents involving medical devices. Compliance with national and international health regulations.
More safety for patients.
Less risk for the institution.
Technovigilance management is an essential requirement for hospitals and clinics seeking patient safety, ANVISA compliance, and support for accreditations such as ONA and Joint Commission.
Monitoring adverse events, tracking medical devices, and acting quickly on alerts cannot depend on manual or decentralized processes. Neovero Vigilance automates technovigilance alert management and connects your clinical engineering to a secure, traceable, and auditable process.
Audit-ready.
Efficient for everyday operations.
Neovero Vigilance directly supports patient safety, risk management, and regulatory compliance requirements, strengthening audits and accreditations without increasing teams' operational workload.
Segurança do paciente em primeiro lugar
Neovero Vigilance directly supports patient safety, risk management, and regulatory compliance requirements, strengthening audits and accreditations without increasing teams' operational workload.
Patient safety first
Critical alerts made visible and prioritized before they become adverse events — a proactive, not reactive, process.
Compliance without extra effort
Records automatically generated with every analysis — ONA, Joint Commission, ISO 55001, and ANVISA — always ready for inspection.
Automate, standardize, and gain efficiency
Request a demo of Neovero Vigilance and see how your team can manage critical medical devices with safety, compliance, and efficiency — without increasing operational workload.