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.


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.


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!


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: The CFDA Issues an Announcement regarding the Filing of Records for Clinical Trials of Medical Products and Devices

Certain medical products and devices are required to have registration of medical devices approval by the China Food and Drug Administration (CFDA, Chinese: 国 家 食 品 药 品 监 督 管 理 总 局 ) before they can be imported, bought, sold, used or traded in China. There have been many changes and revisions within the Chinese regulatory framework of the CFDA regulations in an effort to ensure the safety and effectiveness of medical products for the Chinese market.

The CFDA issued an announcement regarding the filing of records for clinical trials of medical products and devices. The goal is to standardize the record filing of clinical trials and to improve the supervision and management of medical device clinical trials.
Portrait of two surgeons wearing surgical masks in the operating

The CFDA recently issued the Measures for Unannounced Inspection of Drugs and Medical Devices, which will take effect on September 1, 2015. The measures provide that development, production, operation and the processing of drugs and medical devices are included in the scope of unannounced inspections. The goal of these inspections is to make sure that that manufacturers stay up to date with the current regulations and to support the positive development of China’s medical equipment industry, guaranteeing the quality and safety of medical products. It is expected that there will be more announcements, reforms and updates to the CFDA regulations in future.

In our News section on our website, we will keep you informed regarding the official announcements and changes to these regulations.

Please do not hesitate to call (UK: +44 2071931135, Rest of Europe: +49 69 2713769150, US: +1 773 654-2673) or Email and we will be happy to answer questions.