注册检验 Production Registration

翔康技术注册员工均为相关产品标准技术委员会的注册会员，每年定期参加CFDA组织的产品技术要求、标准研讨会，熟悉医用电气设备安全通用要求、医疗器械生物学评价要求等各种国家标准及行业标准和检定规程。致力于医疗器械和诊断试剂类产品的国内外标准以及法规的研究，并且与各省局医疗器械检测中心保持良好合作关系，为您提供医疗器械及诊断试剂类产品全方位的注册解决方案！

Xiangkang
Biotech registrars are all registered members of relevant product standards
technical committee. They regularly participate in the product technical
requirements and standards seminar organized by NMPA every year. They are
familiar with various national standards and industry standards and
verification regulations, such as general safety requirements for medical
electrical equipment and biological evaluation requirements for medical
devices. Committed to the domestic and foreign standards and regulations of
medical devices and diagnostic reagent products, and maintain a good
relationship with provincial medical device testing center, to provide you with
a full range of medical devices and diagnostic reagent products registration
solutions.