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 compliance consultant and expert. Adhering to the corporate philosophy of "Professionalism, Integrity, and Win-Win," Zhongmiao Inspection showcases professionalism, treats people with sincerity, collaborates with industry peers, shares knowledge, provides value-added services exceeding customer expectations, and grows together with clients and peers!

Primary Business Activities ：

Medical Device Domestic Registration and Certification Consulting：Medical Device Registration, Medical Device Production License, Medical Device Production Record, Import Medical Device Registration and Record, ISO9001 and ISO13485 System Certification Consulting.

Medical Equipment GlobalRegisteredCertification Consulting：EU CE Certification Consultation, USA FDA Registration, Customs Union EAC Certification Consultation, 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, US FDA Regulation Training, ISO 13485 System Training, Domestic Medical Device Related Regulations Training.

Section 4: Adjacent ServicesFood:BRC factory audit, FDA GMP audit, FCE-SID registration, FDA registration;MedicationsFDA OTC Registration, FDA NDC Registration, FDA OTC Pre-Review, FDA OTC Factory AuditCosmeticsFDA Registration, FDA GMP Audit, ISO 22716