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HANGZHOU SHANZE BIOPHARMACEUTICAL CO., LTD.

Germany

European Operations Center

Singapore

Asian Operations Center

Beijing

Regional Operations Center

Shanghai

Regional Operations Center

Hangzhou

China Operations Headquarters

Guidelines for Reporting Adverse Drug Events

If you wish to report an adverse event or a product quality issue following the use of our products, please contact your doctor or pharmacist, or contact us directly using the following methods.

Please send an email to our Pharmacovigilance Department at:safety@shanzebio.com,with a copy to the Quality Department at:quality@shanzebio.com. Please include your name, contact information, and a brief event description in your report. In compliance with applicable laws and regulations, relevant patient information and data will be disclosed only to Shanzebio’s relevant departments responsible for adverse drug reactions. We will follow up with the reporter regarding this event, record the information in Shanzebio’s pharmacovigilance database, and report it to the relevant national regulatory authorities as required by law.

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