FDA(Food and Drug Administration) is the national health authority to protect American consumers and the principals to operate National Health Law. The food we eat is safe, hygienic and cosmetics we use are safe and effective medical devices such as microwave radiation is generated and the device is harmless to the FDA's job to make sure. For a dog or livestock forage will be investigated by the FDA

K-GMP has signed for a strategic MOU with Registrar Corp to expand our expertise to international approval as well as MFDS (Apr. 2013)
It promotes the fastest access for FDA compliance to 8,000 companies over Food & Beverages, Drugs, Cosmetics, and Medical Devices
To build up internal DB

CFDA is the national health authority to protect Chinese consumers and the principals to operate National Health Law. Draft laws, regulations and rules and policy plans on the administration and supervision of food safety, drugs, medical devics and cosmetics formulate normative documents, and facilitate the establishment and iplementation of the food safety responsibility mechanism, under which food companies shall bear the main responsibility and local people's governments shall take integrated responsibility; establish the direct reporting system for oritical food and drug infomation and supervise its impiementation; take measures to reduce risks on regional and systemic food and drug safety.

The principal point of CE marking is to provide a 'level playing field' of market requirements across the European Community. Effectively, this removes barriers to trade throughout the European Economic Area, allowing companies free access to markets in all the different countries without having to meet particular local requirements.

CE.way is a regulatory consultancy firm providing European Authorized Representative and EU Responsible Person services.
At the core of operations we provide regulatory services primarily for the cosmetics and medical device industries.

We guarantee the high-quality services. When manufacture of importer/exporter submits allocation for manufacturing of importing/exporting business approval of medical device, the manufacturer or importer/exporter should simultaneously submit at least one application for product notification or product approval (manufacturing or importing) of medical device.

The Summary Technical Document (STED) format for regulatory submissions is a harmonized submission format developed by the Global Harmonization Task Force (GHTF), a voluntary partnership of government and industry representatives. GHTF promotes international harmonization of medical device regulation through the preparation and distribution of guidelines such as the proposed STED format.

Legislation may seem complicated, but we are trying to make it easy for you. Our aim is to answer all your questions, eliminate all concerns and help you make an informed decision, If you would like a consultation or an offer for our services just state the requested details below and we will explain all the requirements for you.