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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CFDA

Cosmetic products and medical devices need a CFDA registration before they can be sold in China. We offer the evaluation of CFDA classifications (Class I – III) for the medical devices, and guide you through the complete approval processes.

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.

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 Announces 90 Additional New Industry Standards for Medical Products

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 sold or used in China. In an effort to insure continued safety and effectiveness of medical products, there have been numerous changes and revisions within the Chinese regulatory framework for CFDA certification.

In March of 2014 the CFDA published a completely new version of the “Regulations for the Supervision and Administration of Medical Devices” (Chinese: 医疗器械 监督管理条例(修订草案).

Previously in our “News” section we informed you (“CFDA Announces 120 New Industry Standards for Medical Products”) that the CFDA introduced 120 new Industry Standards (abbreviated as “YY Standards”) in announcement No. 30 dated July 3, 2014.

On April 8, 2015 the CFDA has released announcement No. 8 which introduced another 90 new Industry Standards for medical products. The announcement includes 14 mandatory and 76 recommended industry standards. The issuance of these changes will further improve the medical device standards system of China and help improve the overall quality of medical devices.
Portrait of two surgeons wearing surgical masks in the operatingThe new standards apply to the following products:

  • Implants for surgery
  • Medical electrical equipment
  • In vitro diagnostic reagents
  • Dentistry

The purpose for these changes is to promote the positive development of China’s medical equipment industry and to ensure the quality and safety of medical products. It is expected that there will be more announcements, reforms and changes to the CFDA regulations in the future. In our “News” section on our website, we will keep you informed regarding official announcements and changes to the regulations.

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 or email with any questions you may have.

 

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