ADVERSE EVENT REPORT

VIRILABS takes product safety seriously. In compliance with FDA guidance under 21 CFR 820.100, we maintain a system for collecting, evaluating, and reporting adverse events related to our research products.

How to Submit a Report

If you observe an adverse event in a laboratory research setting related to a product purchased from VIRILABS , please complete the form below. We will acknowledge your report within 24 hours.

Required Information for Your Report

Please include the following in your submission:

Product name and lot/batch number (found on your COA)
Date of the event
Description of the adverse event observed in the research setting
Research subject type (in vitro, animal model, etc.)
Your contact information

Our Response Process

Acknowledgment of receipt: within 24 hours
Internal review: within 5 business days
FDA notification: within the statutory 15-day window where applicable