China Register Category
　

Top Articles
  • The procedure for Import Drug SFDA Registration
  • CFDA Releases Plan to Improve Medical Device Adverse Event Monitoring
  • Our Services for IDL(Import Drug Licence) of SFDA
  • China Supervision and Inspection of Drugs
  • Application and approval procedure for drugs(2)
  • China Launches Review of Medical Device Industry
  • The drugs which can be exempted from clinical trials in China
  • CFDA Reduces Application Requirements for Medical Device License Amendment and Renewal Processes
  • CFDA Issues Guide for Routine Inspections of Medical Device Manufacturers
  • CFDA Issues Proposed Regulations on Medical Devices
  • China Hygiene Supervision and Inspection of Food
  • Application and approval procedure for clinical trials
  • Our Services for IPEL (Import pharmaceutical excipient Licence)
  • China Import Control on GM Agricultural Bioproducts
  • Requisite documents of Drugs SFDA Registration
    		•
    　

    Latest Articles
  • China Hygiene Supervision and Inspection of Food
  • China Supervision and Inspection of Drugs
  • China Supervision and Inspection of Mechanical and Electrical Products Regulations.
  • China Import Control on GM Agricultural Bioproducts
  • China Customs Clearance for Goods Subject to Entry-exit Inspection and Quarantine
  • What is AQSIQ of China?
  • China Issues Special Procedures for Innovative Medical Devices
  • CFDA Issues Guide for Routine Inspections of Medical Device Manufacturers
  • CFDA Releases Draft Good Supply Practices for Medical Devices
  • CFDA Reduces Application Requirements for Medical Device License Amendment and Renewal Processes
  • CFDA Releases Plan to Improve Medical Device Adverse Event Monitoring
  • China Launches Review of Medical Device Industry
  • China Reorganizes the State Food and Drug Administration and Appoints a New Commissioner
  • China FDA Seeks to Improve Medical Device Evaluation at the Provincial and Municipal Government Levels
  • CFDA Publishes Draft Rule on Administrative Procedure for Public Comment
    		•
    　

    　

    　

    　
    　
         Home >> China Regulations News
    　

      The categories of import drugs in China

    ADD DATE:2010-2-20 HITS:6

    According to the Regulations on drug registration of China, the import drugs are specified as three general categories:

    1. Chemical Drugs

    Category 1: The chemical drug never being marketed in any country /region all over the world and the ex-China clinical trials being at least in the stage of Phase II .

    Category 3: The chemical drug being marketed in some country (region)(no matter in China or ex-China), and marketing approval obtained in its country/region of manufacture.

    2.  Herbal Medicines/ Botanic Medicine

    Being omitted because they are too intricate to come to a brief introduction, if you want to know more about these, please contact us and send us an introduction of your products, we will investigate it and then tell you what the categories your products belongs to.

    3.  Biological Products

    Being omitted because they are too intricate to come to a brief introduction, if you want to know more about these, please contact us and send us an introduction of your products, we will investigate it and then tell you what categories your products belongs to.
    　
    Similar topics:

    　

       >> Contact a RJS expert for more information >>

    　
    　
    　 　
    　

    | +86-400-657-8191 | Guangdong:+86-755-25831330 | Beijing:+86-10-51663836 | Shanghai:+86-21-31255165  |

    RJS MedTech Inc.  ©  Copyright 2000-2015 All Rights Reserved