In case you have experienced any adverse event related to the use of the Linde Healthcare products and orservices, please fill out the form below with as much detail as possible. Our top priority is to ensure the safety andsatisfaction of our customers, users and patients. Thank you for your continued trust in us.
Data Protection Notice for Adverse Event Reporting
We process the personal data you submit to us in the course of the adverse event reportina solely for the for the purposes of monitorina the safety oidruas / medicinal products and medical devices. This includes but is not limited to the assesing and preventing of adverse events as wellas thereporting of advese events to national and international health authorities or other institutional authorities in accordance with applicable laws anrequlations. We may respond and follow up with you on your report and may provide the personal data to those linde employees and third partiewho 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 pesonal data s in accordance with applicable laws and reaulationsFor further information, includina but not limited. onwho is responsible for the processing of your data and your rights you can find under information on data protection.
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