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Grzan Medical Technology (SZ) Co., Ltd subordinate to Grzan group, is a holding subsidiary of Grzan group. Grzan medical specializes in customized regulations and registration consulting services for medical devices and in vitro diagnostic products, and provides training services for regulations and standards. Specific service areas include: EU CE certification consulting for medical devices (IVDD, MDR, IVDR), clinical experiment, ISO13485 system certification consulting, FDA registration consulting (including 510k, QSR 820, etc.) Product inspection and rectification consultation (electromagnetic compatibility, electrical safety, performance, biocompatibility, wireless, packaging test, etc.); Domestic registered nmpa consulting services (clinical scheme cro consulting services, product registration certificate consulting services, production license consulting services, import registration consulting services).
Grzan News
Tel：0755-33509057
Adress：Room 103-108, Building B, Block 2, Bangkai Science and Technology Park, No. 9, Guangyuan 5th Road, Fenghuang Street, Guangming District, Shenzhen City, Guangdong Province, China.
E-mail：hitolin@grzan.com
Grzan medical can undertake the whole process of technical guidance and services such as prospective clinical, who Eul, variant virus research (Delta, Omicron ba.1, ba.2), IVDD CE, ivdr CE, Australian TGA, British CTDA, European HSC common list, European service, British service, etc.
If you have products that have been tested and certified or want to know more about them, please contact Grzan medical！
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