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 Issues Three Appendixes for Good Manufacturing Practice for Medical Devices

The China Food and Drug Administration (CFDA, chin: 国家食品药品监督管理总局) recently formulated and issued three appendixes for good manufacturing practice for medical devices. The purpose is to strengthen the supervision and management of medical devices, improve enterprises’ quality management level, and to ensure the safety and effectiveness of medical devices.

The three appendixes on Promulgation of Good Manufacturing Practice for Medical Devices are the following:

  1. Appendix for Sterile Medical Devices (No. 101 Announcement of 2015)
  2. Appendix for Implantable Medical Devices (No. 102 Announcement of 2015)
  3. Appendix for In Vitro Diagnosis Reagents (No. 103 Announcement of 2015)

These appendixes were created in accordance with the “Regulations for the Supervision and Administration of Medical Devices” (chin: 医疗器械 监督管理条例(修订草案) (State Council Decree No. 650) and the Administrative Measures for the Supervision of Medical Device Manufacturing (CFDA Order No. 7).

In the three appendixes, there is particular emphasis on the Good Manufacturing Practice of sterile medical devices, implantable medical devices and in vitro diagnosis reagents, which will come into effect as of October 1, 2015.
Chinese Female Woman Scientist & Microscope In LaboratoryIt is expected that there will be more announcements, reforms and changes to the CFDA regulations in the near future. In our News section on our website, we will keep you informed regarding the official announcements.

If you want to learn more about CFDA certification for medical devices and products, please visit the CFDA section on our website. We also provide more detailed knowledge regarding CFDA in our free brochure “CFDA China – The Booklet” that can be downloaded here.

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.