Adverse Event

Adverse event reportng

Adverse Event Reporting

In case you have experienced any adverse event related to the use of products and/or services, please fill out the form below with as much detail as possible. Our top priority is to ensure the safety and satisfaction of our customers, users and patients. Thank you for your continued trust in us. 
Information on the reporter
Information on the patient
Information on the product concerned
Description

We process the personal data you submit to us in the course of the adverse event reporting solely for the purposes of monitoring the safety of drugs / medicinal products and medical devices. This includes but is not limited to the assessing and preventing of adverse events as well as the reporting of adverse events to national and international health authorities or other institutions and authorities in accordance with applicable laws and regulations. We may respond and follow up with you on your report and may provide the personal data to those Praxair employees and third parties who are involved in the assessing, preventing and reporting of adverse events or need to be informed about the adverse event.

The retention time for your personal data is in accordance with applicable laws and regulations.

Further information, including but not limited, on who is responsible for the processing of your data and your rights you can find under Information on data protection.

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