Advers Event & Quality Issue Reporting

Reporting an Adverse Event will help VSY Biotechnology GmbH track the safety of all our biotechnology products to ensure that are completely safe for patients and healthcare professionals who use them.

Adverse Event reports allow us to unsure up to date information on our products and devices in the instruction for use and product information leaflets to help minimise risk and maximise benefit to the patients. We continuously monitor the safety and performance of all of our products through our postmarket surveillance process.

It is important to report adverse events even if it is a known adverse event as this still provides valuable information for monitoring product safety

For adverse event reporting

Please refer infomation available in this form for the requirements of European Medical Device Regulation (MDR) and MDSAP Programme: Summary of vigilance requirements across MDSAP and the MDR

OR

Please contact us to report an adverse event at: complaint@vsybiotechnology.com

For quality issues

Please submit your questions about the quality of an VSY Biotechnology GmbH products through this form:

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