Company Profile

Zhongmiao Inspection Technology (Shanghai) Co., Ltd. was established in the free and open city of Shanghai, China, and is a specialized technical service company focusing on domestic and international medical device registration and certification. We offer a one-stop compliance service solution for medical device clients, becoming their on-site compliance consultant experts. Adhering to the corporate philosophy of "Professionality, Integrity, and Win-Win," Zhongmiao Inspection showcases professionalism, treats people with sincerity, collaborates with industry peers, and provides value-added services exceeding client expectations. Together with clients and peers, we grow hand in hand!

Primary Business ：

Medical Device Domestic Registration and Certification Consultation：Medical device registration, medical device production license, medical device production filing, import medical device registration and filing, ISO9001 and ISO13485 system certification consultation.

Section II: Medical Devices WorldwideRegisterCertification Consulting：EU CE Certification Consultation, US FDA Registration, Customs Union EAC Certification Consultation, South Korea KFDA Registration, Brazil ANVISA Registration, Japan JPAL Registration, Canada HC Registration, Free Sale Certificate, MDSAP Registration.

Section 3: Medical Device Legal and Regulatory Training：EU CE Regulation MDR Training, EU CE Regulation IVDR Training, US FDA Regulation Training, ISO 13485 System Training, Domestic Medical Device Related Regulation Training.

IV. Adjacent Business Activities:Food:BRC factory audit, FDA GMP audit, FCE-SID registration, FDA registration;MedicinesFDA OTC Registration, FDA NDC Registration, FDA OTC Pre-Review, FDA OTC Factory AuditCosmeticsFDA Registration, FDA GMP Audit, ISO 22716