Swiss FINMA warnings List
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2,169 Entities in Swiss FINMA warnings List
Entity Name | Entity Type | Effective Date | Status |
---|---|---|---|
Exton Global | Company | May 10, 2024 | inactive |
LGT International Group HK Co Ltd und LGTFX Group | Company | Jan 16, 2023 | inactive |
Vital Group Assurances SA | Company | Dec 23, 2024 | active |
Werte Consulting AG | Company | Jan 16, 2023 | inactive |
Dynamic Capital Group AG | Company | May 26, 2023 | inactive |
Rextura Limited | Company | Aug 14, 2023 | inactive |
Havel Hightec AG | Company | Sep 27, 2022 | inactive |
Havel Hightec AG | Company | Jan 16, 2023 | inactive |
Koya Trading Europe | Company | Jan 16, 2023 | inactive |
Kaizen Tech Limited | Company | Sep 21, 2023 | inactive |
FAQs
Why is compliance with the Suspended and Revoked Manufacturing and Wholesale Distribution Authorisations by MHRA necessary?
Compliance with suspended and revoked manufacturing and wholesale distribution authorizations issued by the MHRA is crucial to ensure the safety and efficacy of pharmaceutical products. These sanctions are put in place to protect public health by preventing non-compliant entities from operating. Adhering to these regulations safeguards against potential risks associated with substandard or unsafe medicinal products, promotes trust in the healthcare system, and maintains the integrity of the supply chain. Non-compliance can lead to serious legal consequences and harm to patients.
Which companies should comply with Suspended and Revoked Manufacturing and Wholesale Distribution Authorisations by MHRA?
Companies in the pharmaceutical, biotechnology, and medical device sectors must comply with the regulations governing suspended and revoked manufacturing and wholesale distribution authorisations by MHRA. Compliance is crucial to ensure the safety and efficacy of products, protect public health, and maintain ethical standards. Non-compliance can lead to severe penalties and harm the company’s reputation and operational capabilities.
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