Automotive CCC

China Certification is an excellent partner for the CCC certification in the automotive sector. We are providing leading automotive suppliers and car manufacturers with quick and smart solutions for their CCC certification. We offer you our support for every project related to the Automotive CCC.

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CCC Made Easy

The China Compulsory Certification (CCC) is a mandatory certification for products exported to China.
We are experienced in the CCC certification process for all kinds of product categories. The CCC certification process will be simple and easy with China Certification Corporation as a professional partner by your side.

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Other Certifications

HAF604, Taiwan Certification, CRCC for Railway Products, SRRC Type Approval, NAL (Network Access License), AQSIQ registration, Voluntary CQC Mark Certification, CCCF for Fire Products: We support you in all types of certifications for the Chinese market.

Consulting

China Certification provides a range of specialized consulting services, especially for car manufacturers and large industrial companies. With the consulting packages the certifications as well as internal procedures related to international product certifications can be streamlined.

TRAINING

China Certification Corporation offers customized CCC training to fit your company needs. Our trainer will come to your location and provide the training, up to date information and pass on valuable tips from our many years of experience. Call us today to learn more!

Company

Since 2005, MPR China Certification GmbH – China Certification Corporation has been supporting companies around the world in obtaining the required product certifications for the Chinese market. With a strong team located worldwide, we can offer you the best solution for your enquiries.

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CFDA: CFDA Issues Rules for Classification of Medical Devices

Certain medical products and devices are required to have prior approval by the CFDA (China Food and Drug Administration Chinese: 国家食品药品监督管理总局) before they can be imported, bought, sold, traded or used in China. In an effort to insure continued safety and effectiveness of medical products there have been ongoing changes and revisions within the Chinese regulatory framework for CFDA certification.

The CFDA recently issued the Rules for Classification of Medical Devices (Order No. 15), which will be implemented as of January 1, 2016.

The new order discusses how risk-based classification of medical devices will be used not only for registration but also for device production and supervision. This includes revisions and clarifications to classifications, terms, and definitions of medical products and devices.
Team of surgeons in the operating room, female surgeon holding s

It can be difficult for medical device manufacturers to determine if their products will require certification, and if so, in which classification their products should be categorized.

A complete evaluation of CFDA-responsibility and classification simplifies your registration process and prevents additional, unplanned costs.

If you have any questions or concerns, please do not hesitate to Email or call us: Germany: +49 69 271 3769 150, UK: +44 2071931135, US: +1 773 654 2673

 

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