详情描述





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
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