Report adverse events

THIS SITE IS NOT INTENDED OR DESIGNED FOR REPORTING OF ADVERSE EVENTS

ViroGates is required to document reports of adverse events, both for comprehensive safety monitoring of its products and also to fulfill reporting requirements to Regulatory Authorities. It allows continued monitoring of the benefit/risk balance of the medicinal product.

Adverse events should be reported. Reporting forms and information can be found at fda.gov or through the FDA Adverse Event Reporting System (FAERS). Adverse events should also be reported to ViroGates A/S. Please contact ViroGates Adverse Events by emailing adverse.events@virogates.com or calling +45 2113 1336.

Please provide the brand name and batch number, where possible. It is very important that safety surveillance is carried out on a brand/product specific basis to ensure the information collected is accurate.

Date of preparation: January 2021

1000+

published suPAR studies in leading medical journals

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The suPARnostic® brand consists of four products:

suPARnostic POC+

Quick Triage

A Point of Care Solution

TurbiLatex

For Automated Systems

ELISA Assay

Clinical and Research

POC+

Point-of-care finger prick

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