Recently, the VISTA™ Precipitome aneuploidy and copy number variants detection kit product independently developed by BGI was reviewed and evaluated by the Notified Body and officially obtained the CE-IVDR certificate issued by TÜV SÜD Product Service Co., Ltd. On the clinical product side, it indicates that the safety, efficacy and quality management system of this product have been officially recognized by the EU's authoritative notification body, which will further enhance its comprehensive competitiveness in the European Union, the EEA market and other countries and regions that have approved CE-IVDR certification.

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