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 and become their compliance consultant 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 customer expectations. Together with our clients and peers, we grow hand in hand!

Primary Business ：

One. Medical Device Domestic Registration and Certification Consultation：Medical device registration, medical device production license, medical device production record, import medical device registration and record, 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 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 Relevant Regulation Training.

Section 4: Adjacent BusinessFood:BRC factory audits, FDA GMP inspections, FCE-SID registration, FDA registration;PharmaceuticalsFDA OTC Registration, FDA NDC Registration, FDA OTC Pre-Review, FDA OTC Factory AuditCosmeticsFDA Registration, FDA GMP Audit, ISO 22716