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      About Us
RJS MedTech Inc. is a leading Chinese market access consulting company, who's profession is china Administration Departments (NMPA-CFDA, AQSIQ, CNCA, CIQ, MOA, MOH etc.) pre-market approval consulting services. We are engaged in the fields of registration service almost 15 years. We have local offices in Shenzhen, Beijing, Shanghai and Agent in USA.

RJS MedTech Inc. has assisted dozens of foreign manufacturers, hundreds of Products obtained their market access license,Smooth import to China. The clients including United States, Canada,Germany, Switzerland, United Kingdom, France, Italy, Belgium, Spain, Netherlands, Japan, India, Australia, New Zealand, South Korea, Singapore, Brazil, Malaysia, Philippines, Russia, Taiwan, Hong Kong, and other European, American, Asian countries and regions.

RJS MedTech Inc. has rich professional resources and powerful technical efficiency, and also has good communications and relationships with national & local administrative management departments , the clinical trial base and the test institution at different levels, as well as the professional technological guidance from the judging commission and specialists. With good brand reputation, we firmly believe that our sincerity can create a promising future.

     The total solution of import to China !                   

                 Your success in China is our goal !

    Pharmaceuticals NMPA (CFDA) RegisterMore>>    Excipient & Packaging RegisterMore>>

  • china import drug license (NMPA-CFDA approval certificate)
  • Cost & Time for Drug China NMPA (CFDA) Registration (Clinical Trials Permission (CTP) Phase)
  • Cost & Time for Drug China NMPA (CFDA) Registration Approval(Clinical Trials Phase)
  • Cost & Time for Drug China NMPA (CFDA) Register(Import Drug Licence (IDL) approval Phase)
  • China Chemical Drug Registration classification regulations
  • Our Services for IDL(Import Drug Licence) of china NMPA (CFDA)
  • The categories of import drugs in China
  • Requisite application documents for Drug NMPA (CFDA) Approval

  • Pharmaceutical packaging material and container register certificate (China NMPA -CFDA approval license)
  • Pharmaceutical Excipient license(China NMPA -CFDA registration certificate)
  • Pharmaceutical Excipient IPEL china NMPA (CFDA) register Cost & time
  • Pharmaceutical Excipient china NMPA (CFDA) register application documents
  • Pharmaceutical Excipient Export to China Process
  • Cost and Time for Pharmaceutical packaging China NMPA (CFDA) Registration
  • Application documents for Pharmaceutical packaging China NMPA (CFDA) register
  • What kind of Pharmaceutical packaging need NMPA (CFDA) approval?

  •     Medical Device NMPA (CFDA) RegisterMore>>    IVD Reagent NMPA (CFDA) RegisterMore>>

  • China import medical device registration certificate(NMPA -CFDA approval license)
  • Medical Device SFDA Registration Procedrue Flow Chart
  • Introduce of China Medical Devices Market
  • Phases and Time of Medical Devices SFDA Registration
  • Which Medical Devices require to Clinical Trial before SFDA approval
  • SFDA Medical Devices Classification
  • Requisite data of Medical Device SFDA Registration
  • Requisite data of Medical Device SFDA Re-Registration

  • Cost and Time for IVD China NMPA (CFDA) Registration
  • Clinical trial requirements for IVD China NMPA (CFDA) Approval
  • Sample requirements for IVD Type test of China NMPA (CFDA) Registration
  • Application Dossiers of China NMPA (CFDA)  Approval for IVD Products
  • China will be the Second Largest IVD Market by 2017
  • Related Laws and Regulations about IVD Approval in China
  • Classification of In Vitro Diagnostic Reagents(IVD) in China
  • IVD (In Vitro Diagnostic) in China

  •     Imported Food & Supplements More>>    Cosmetics NMPA (CFDA) Registration More>>

  • Foreign Dairy Manufacturers China CNCA Registration Procedure Flow Chart
  • Infant Formula Milk Powder NMPA (CFDA) Registration
  • Imported Pre-packaged Food Chinese Labeling CIQ Filing
  • Imported food facility and Exporter AQSIQ register
  • Import Control on (GMO) Genetically modified Agricultural Bioproducts
  • Hygiene Supervision and Inspection of imported Food
  • Health food supplements formula ingredients Pre-analysis service
  • Foreign Food Export to China Process Flow Chart

  • China import cosmetics registration license(NMPA-CFDA approval certificate)
  • SFDA Registration expense and timetable for Special purpose Cosmetics
  • NMPA (CFDA) Registration cost and timetable for General Cosmetics
  • The toxicology test items for new cosmetics raw material of SFDA require
  • New Cosmetics Raw Material SFDA Registration charge and timetable
  • The request of cosmetics product formula china SFDA submission
  • How to declare for multi-color series of general imported cosmetics?
  • How to apply Chinese label for imported cosmetics?

  •     Disinfectant Products MOH registerMore>>    China Clinical Trial CRO ServiceMore>>

  • China NHFPC (MOH) Hygiene license certificate for Disinfectant & Disinfection device registration
  • Cost and Time for disinfectant China NHFPC(MOH) Approval
  • Application documents for disinfectant China NHFPC(MOH) register
  • Procedures of disinfection Products NHFPC (MOH) Registration
  • Disinfectant test items for china NHFPC(MOH) Registration
  • Our Services for disinfectant NHFPC(MOH) registration?
  • What disinfectants export to china need NHFPC(MOH) registration?
  • What disinfection products export to china need NHFPC(MOH) register?

  • CRO & Clinical Trials Services in China
  • Pre-clinical Research Services
  • Clinical Trials in China
  • Medical Documents Translation Service
  • Benefits of INDEPENDENT regulatory representation
  • Main Responsibilities of the SFDA
  • Introduce of China SFDA
  • Introduce of RJS Medical Technology Inc.

  •     China NMPA (CFDA) RegulationsMore>>    Other ProductsMore>>

  • Why not to choose the distributor as your SFDA legal representative agent
  • Drug Administration Law of China
  • Regulations for Implementation of the Drug Administration Law of China
  • Regulations for the Supervision and Administration of Medical Devices
  • Regulations on Administrative Protection for Pharmaceuticals
  • Provisions for Drug Insert Sheets and Labels
  • Provisions for Medical Device Classification
  • Special Review and Approval Procedure for Drug Registration of SFDA

  • China Foods for Special Medical Purpose (FSMP) NMPA (CFDA) Registration Procedure Flow Chart
  • Infant Formula Milk Powder China NMPA (CFDA) Registration Procedure Flow Chart
  • Guide of Infant Formula Milk Powder China NMPA (CFDA) Registration
  • NMPA (CFDA) Registration Application Guide of Foods for Special Medical Purpose (FSMP)

    Important Note
    Due to the reorganization of the Chinese government in 2018,
    CFDA (China Food and Drug Administration) was renamed to NMPA (National Medical Product Administration), and its food supervision function has been transferred to SAMR (State Administration for Market Regulation of China);
    AQSIQ (General Administration of Quality Supervision, Inspection and Quarantine of China) was abolished, and its import and export trade supervision function has been transferred to GACC (General Administration of Customs of China),
    Therefore, all
    CFDA and SFDA on this website default to NMPA, AQSIQ defaults to GACC; 
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