On May 17, 2013 China Quality Certification Centre (CQC) announced they have developed and introduced a voluntary CQC safety certification for child restraint systems. It bases on the existing National Standards GB 27887:2011 (Restraining devices for child occupants of power-driven vehicles) and GB 8410:2006 (Interior trimming material in vehicles). All provisions regarding the certification can be found in the CQC guideline CQC11-491281-2013. Since June 1st, 2013 applications for CQC safety certification of child restraint systems can be submitted to the CQC. At the moment no China Compulsory Certification (CCC) is needed.
You can find more information regarding CCC certification on our website.
With the ever growing hunger for foreign products and the money to pay for them, the Chinese market has become very important for the automotive industry. Understandably, nearly every car manufacturer is focusing more and more on getting their products into China. The only way to legally export a vehicle to China is to obtain CCC certification (China Compulsory Certificate).
The CCC certification process with the Chinese certification authority CQC (China Quality Certification Centre) or CCAP (China Certification Centre for Automotive Products) is needed to deliver to the Chinese market without restrictions. It is important to note that these regulations apply not only the certification of complete vehicles but also affect the automotive suppliers that provide components and spare parts for their customers in China. The relevant regulations are defined in the Chinese National GB Standards (Chinese: Guobiao), which identify the CCC requirement of the vehicle parts and what to which criteria they have to be tested. After the successful CCC certification components and spare parts can export their certified products to China without any risks of delay at Chinese customs.
On November 13th, 2013 Mr. Julian Busch, CEO of China Certification Corporation, has published an article about the CCC certification for automotive parts and complete vehicles. It can be found on the web pages of the German journal “Automobil Industrie”, a professional journal for executives in automotive industry.
The article “China Compulsory Certificate für Automobilteile und Gesamtfahrzeuge” (“China Compulsory Certificate for automotive parts and complete vehicles”) describes the certification process and its challenges.
The article points out that a CCC certification can be completed with professional support within only a few months. The certification process can fast-tracked with careful planning and attention to detail. Thorough preparation of the application documents and the supporting documentation, and close communications with the Chinese test laboratories and Chinese certifying authorities will ensure a successful certification. The article is available online here (only in German language).
Information about CCC certification, the process and the costs can be found on our website. For a general overview of the certification process please download our free brochure “CCC Made Easy”. More detailed information can be found in our book ” A Brief Guide to CCC: China Compulsory Certification” which can be ordered directly on Amazon.
Please also take a look at our reference page on our website to get a better idea of our clientele and what they are saying about us.
We offer Customs Clearance for smooth export of your products into China. We will take care of the complete customs clearance and can resolve any issues regarding certification requirements, reducing the risk of your goods being held in customs. For more detailed information regarding customs clearance in China, possible import problems, permitted exemptions and our service package you can download our free booklet “Customs clearance China”.
China Certification Corporation also offers assistance in obtaining CEL (China Energy Label) for certain electrical appliances, and CDFA (China Food and Drug Administration) for medical devices. You can find more information regarding our complete list of services on our website.
Please do not hesitate to call or email with any questions you may have.
Mr. Julian Busch, CEO of China Certification Corporation, has published an article about the approval of medical devices for Chinese market. It was published in the November 2013 issue of the German journal “DeviceMed”, a professional journal for manufacturers of medical products and devices. The article “CFDA – Nicht nur der Name ist neu” (“CFDA – not only the name is new”) informs about the renaming and reorganization of the CFDA, describes the regulatory process of CFDA certification and points out the potentials of the Chinese market for medical devices. The article is also available online (only in German language) here.
You can find more information about CFDA registration here.
The CFDA has developed a standard for electromagnetic compatibility (EMC) of medical devices to insure safety. This industry standard YY0505-2012 corresponds to the International standard IEC 60601-1-2 (Medical electrical equipment Part 1-2: General requirements for basic safety and essential performance – Collateral standard: Electromagnetic compatibility – Requirements and tests) and the Chinese Standard GB 9706.1-2007 (Medical electrical equipment – Part 1: General requirements for safety). The industry standard YY0505 2012 was announced in December 2012 and will be implemented from the 1st of January 2014 as a mandatory industry standard for electrical medical devices in the Peoples Republic of China.
You can find more information about CFDA registration here.
Certain medical products and medical devices must be certified and registered by the China Food and Drug Administration (CFDA) before they can be exported to China. Until recently, CCC certification at CQC was also required for some of these products. The AQSIQ changed this policy with “Announcement 52” in April 2013, no longer requiring CCC certification (with the CQC) for medical products and devices as of May 2013. All certification for medical products and devices now falls under the CFDA certification and registration process.
This change affected the following devices: Implantable Pacemakers, Rubber Condoms, ECG Devices, Artificial heart-lung Machines, Extracorporeal Blood Circuit for Blood Purification Equipment, Hollow Fiber Dialyzers, Hemodialysis Equipment, Medical Diagnostic X-Ray Equipment.
Please click here for more information about CFDA.