Home    CFDA Registration   AQSIQ Register   CIQ Inspection   CNCA Registration   NHFPC(MOH) Register   MOA Register      Contact Us

 Guide of How Export China
   
 
CFDA
CFDA registration
AQSIQ
AQSIQ registration
CIQ
CIQ registration
CNCA
CNCA registration

Foods  Products

Dietary Supplements

Infant Formula

Food for Special Medical Purpose

Dairy Products

Meat & Aquatic Products

Wine & Liquor

Pet Food

Cosmetics

Medical Device

Drug Medicine

Electronic Products
 
 
      About Us
RJS MedTech Inc. is a leading Chinese market access consulting company, who's profession is china Administration Departments (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 CFDA RegisterMore>>    Excipient & Packaging RegisterMore>>

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


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

  •     Medical Device CFDA RegisterMore>>    IVD Reagent CFDA RegisterMore>>

  • China import medical device registration certificate(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 CFDA Registration
  • Clinical trial requirements for IVD China CFDA Approval
  • Sample requirements for IVD Type test of China CFDA Registration
  • Application Dossiers of China CFDA (SFDA) 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 CFDA Registration More>>

  • Foreign Dairy Manufacturers China CNCA Registration Procedure Flow Chart
  • Infant Formula Milk Powder 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(CFDA approval certificate)
  • SFDA Registration expense and timetable for Special purpose Cosmetics
  • 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 CFDA(sfda) 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) CFDA Registration Procedure Flow Chart
  • Infant Formula Milk Powder China CFDA Registration Procedure Flow Chart
  • Guide of Infant Formula Milk Powder China CFDA Registration
  • CFDA Registration Application Guide of Foods for Special Medical Purpose (FSMP)

  •  
    Similar Topics
     Top Articles
      Search Tools
    China National GB Standards Search
    China HS Code Search
    Customs Tariff & Tax Search
    CIQ Import Inspection Requirements Search
    China Cosmetics Formula Ingredients Analysis Systemm 
    China Foods Formula Ingredients Analysis System
    Contact Us
    Post Message
    info@sfdachina.com 
    rjschina
    +86-400-6578191
    *Order Items
    *Payment Amout USD
    *Email
     
     
      |  Home  |  About Us  |  Our Service   |   China Regulations News  |  Contact Us  |

    +86-400-6578191        info@sfdachina.com 
    106# Zhongmao Mansion,No.1 Beizhan Road, Shenzhen,China 518000
    ©  RJS Copyright  2001-2017 All Rights Reserved



    www.GBstandards.org