Company Profile

Zhongmiao Inspection Technology (Shanghai) Co., Ltd. was established in the free and open city of Shanghai, China, as a technical service company specializing in domestic and international medical device registration and certification. We offer one-stop compliance service solutions to medical device clients and become their compliance advisor experts. Adhering to the corporate philosophy of "Professionalism, 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 Consulting：Medical device registration, medical device production license, medical device production filing, import medical device registration and filing, ISO9001 and ISO13485 system certification consultation.

Section 2: Medical Equipment WorldwideRegisterCertification Consulting：EU CE Certification Consultation, US FDA Registration, Eurasian Economic 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 Regulatory Compliance Training：EU CE Regulation MDR Training, EU CE Regulation IVDR Training, U.S. FDA Regulation Training, ISO 13485 System Training, Domestic Medical Device Relevant Regulation Training.

Section 4: Adjacent Business OperationsFood:BRC factory audit, FDA GMP inspection, FCE-SID registration, FDA registration.MedicinesFDA OTC Registration, FDA NDC Registration, FDA OTC Pre-Review, FDA OTC Factory AuditCosmeticsFDA registration, FDA GMP factory audit, ISO 22716