{"id":1466,"date":"2025-05-15T11:13:11","date_gmt":"2025-05-15T10:13:11","guid":{"rendered":"https:\/\/helsinn-demo.it\/?page_id=1466"},"modified":"2025-05-15T14:44:31","modified_gmt":"2025-05-15T13:44:31","slug":"contact-us","status":"publish","type":"page","link":"https:\/\/helsinn-demo.it\/en_us\/contact-us\/","title":{"rendered":"Contact Us"},"content":{"rendered":"
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PRIVACY STATEMENT<\/h4>

The provision of personal data by you may be necessary where in our legitimate interest in order for us to provide you with the requested services\/information and for the performance of any contractual relationship with you. Because of our commitment to the protection of your personal data, we evaluate our privacy policies and procedures to implement improvements and refinements from time to time. Please read the\u00a0Privacy and Cookies Policy<\/a>\u00a0carefully in order to understand our views and practices regarding your personal data and how we will treat it. The Privacy and Cookies Policy is also a part of our\u00a0Terms of Use<\/a>\u00a0for the Website.<\/p>

REPORTING OF ADVERSE EVENTS<\/h4>

Patient safety is a priority for Helsinn. We are committed to collect, analyse, and react upon any new information about the benefits and risks of our products. If you have information about a side effect or adverse reaction associated with any of our products, please let us know completing the form at the following\u00a0link<\/u>.<\/a><\/p>

Helsinn is legally required to ensure that adverse events are traceable and available for follow-up. As a result, we must keep information about the reporter (i.e., the person reporting the occurred adverse event) to allow us to contact him\/her once we have received the report, unless the reporter has expressly declined any follow-up contact. The personal data that we may collect when you report an adverse event is your: name; contact details (which may include your address, e-mail address, phone number or fax number); profession, and in case of healthcare professionals it may be asked also the clinic\/institution name and address. All this information may determine any other further questions you could be asked about when you report an adverse event. It must be eventually defined the relationship between you and the subject of the adverse event.<\/p>

Adverse events may also be reported to your national Health Authority as applicable according to national legislation.<\/p>

The data you provide will be processed in full compliance with the applicable data protection laws. For further information please refer to the\u00a0Pharmacovigilance\u00a0Data Privacy Policy<\/u><\/a>.<\/p>

HOW TO ADDRESS COMPLIANCE CONCERNS<\/h4>

If you observe a misconduct please follow this\u00a0link<\/a>.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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