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Mid-Link Technology Testing is a prominent China-based CRO and consulting firm specializing in medical device and pharmaceutical regulatory testing. The company offers a wide portfolio including bench testing, preclinical animal studies, quality audits, and registration services globally. However, as of 2024-2025, the FDA has rejected all data from this facility due to serious, unresolved allegations of falsified and unreliable test data in biocompatibility and animal safety studies, resulting in a suspension of acceptance for all device or drug-related test data submitted to the FDA from this facility.
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