US FDA Certification
US FDA Certification

A great many products exported to the U.S. are required to process FDA certification and EPA certification before entering the U.S. market. Then what do you know about FDA certification and EPA certification? As a leading product safety and regulatory consulting firm, CIRS Group is now able to provide the U.S. FDA certification and EPA certification services to help clients remove the technical barriers to trade and successfully enter the US market.

What is US FDA Certification?

The U.S. Food and Drug Administration (FDA) is one of the executive agencies of the U.S. government under the Department of Health and Human Services (DHHS). As a scientific management agency, the FDA's responsibility is to ensure the safety of food (including food additives), food contact materials (containing additives), medical devices, radioactive products and pharmaceuticals produced or imported in the United States. The above products must be registered or certified by the FDA before they can be sold in the US.

According to the product category, the US FDA certification can be divided into the following categories:

  • Food Facility Registration;
  • Food Contact Substance Notification (FCN);
  • Food contact materials FDA testing;
  • Medical device FDA registration and exemption application;
  • Laser products FDA registration;
  • Voluntary Cosmetics Registration Program (VCRP);
  • Drug FDA registration;

Our Service

  • U.S. FDA and EPA certification consulting and training
  • U.S. FDA and EPA certification
  • U.S. FDA and EPA related testing

Our Advantages

CIRS has owned a wholly-owned subsidiary in the United States and is able to provide EPA and FDA certification. Besides, C&K Testing, subsidiary of CIRS Group in China, has been accredited by the China National Accreditation Service for Conformity Assessment (CNAS) and China Metrology Accreditation (CMA) and can carry out certification-related testing according to global standards.

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