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  • Cisema Webinar on Certification of Medical and Cosmetic products in China (German)

Cisema Webinar on Certification of Medical and Cosmetic products in China (German)

Thursday, 02 April 2020 / Published in Cosmetics, Medical Device, Webinars

Cisema Webinar on Certification of Medical and Cosmetic products in China (German)

Since the outbreak of COVID-19, health care has become even more of a focus. China was already the second largest market for the healthcare sector and the largest consumer of cosmetics worldwide. With double-digit growth figures, the Chinese market continues to show enormous potential for development and continues to rely on high-quality goods from abroad. However, product certifications are a prerequisite for sales in China.

On March 26, 2020, Advantage Austria, together with Ms. Anna King, who has many years of experience in China certification as a consultant for CISEMA, informed about recent regulatory and institutional developments. The webinar took place in the context of the internationalisation campaign go-international.

In addition to details on the process, duration and costs of a certification as well as the choice of a suitable NMPA legal agent, the webinar focused on the restructuring of the authorities and introduced the responsible NMPA. Certification processes and the latest regulatory updates in the area of MedTech and cosmetics were then discussed. For medical devices, UDI (Unique Device Identification) barcodes, product risk classification, factory inspections abroad and clinical trials in China are among the most important topics. “Hot topics” for exporters of cosmetics include animal testing, new mandatory tests and the ban on microplastics.

Missed the webinar?

The video recording of the webinar can be viewed on YouTube. We hope that you will learn some valuable information.

Tagged under: animal testing, Clinical Trials, cosmetics, factory inspections abroad, MedTech, microplastics, UDI, Unique Device Identification

What you can read next

Extension of Exemption List for Medical Devices and IVDs soon
Attend three webcasts with Cisema on February 23 – 25, 2021
Human Factors
Public Consultation on Inclusion of Human Factors for NMPA Medical Device Registrations

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