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Medical Devices
Dedicated to domestic and international drug regulatory research, with decades of experience in drug regulatory research in China, the United States, and Europe, we provide regulatory services such as medical device registration, medical device quality management system certification, market access consultation for innovative drugs, generic drugs, and raw and auxiliary packaging products, product registration declaration, and post market supervision, covering the entire lifecycle of drugs.
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    全方位提供检验检测服务
  • 产品认证
    熟悉国际认证法规和医疗物资全球进出口的贸易要求
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