Discussions

The import of an IVD medical device in India requires compliance with CDSCO regulations. Importers must obtain an import license, ensure product registration, and provide detailed technical documentation, including device specifications, clinical data, and safety reports. The IVD medical device must meet quality standards and labeling requirements. Additionally, importers should follow post-market surveillance guidelines and maintain proper records. Adhering to these regulatory steps ensures that the IVD medical device is legally approved, safe, and effective for diagnostic use in India.

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