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RJS Medical Technology Inc. is a leading Chinese Medical Consulting Company, who's profession is CFDA(sfda)  registration consulting service and market penetrate in China. We have already successfully assisted different foreign medical manufacturer entering China market. We have local offices in Beijing, Shanghai, Guangdong and agent in USA.

RJS Medical Technology Inc. business scope covers medicines, biological products, medical appliances, healthy products, crude drugs , sterilized products, and etc. It provides such services as product research and development, CRO, registration and declaration, technology transfer , the services and consultations of professional policy & technology, the study on market programs & the market , foundation declaration , and the whole course agency for the export and import of medical products for all the customers in the fields.

RJS Medical Technology 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.

RJS Medical Technology Inc. can provide Chinese CFDA(sfda)  registration and CRO services to worldwide clients , including mainland China,  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 Medical Technology Inc. is truly the bridge between the East and the West.

Your success in China is our goal!

 
 
  Our Business Scope:

1. CFDA(sfda)  Registration Consulting Service;

More For any inquiry, our expert team will carefully and responsibly scheme out the registration schedule, meanwhile the approximate cost for your reference. Experts will be separately appointed to compose your product technical standard and arrange the sample testing as the required by CFDA(sfda) . Basing on strict quality control, we make the documents more qualified, as well as make the appliance easier to pass the inspection of CFDA(sfda)  officials.

2. Regulatory consulting for import medical device, cosmetic, pharmaceutical;

 More We focus on the medical products accessing into China market, help to evoluate medical market in China, meanwhile provide related service for you.

 3. Medical Documents Translation;

More RJS's highly qualified translators include those with Master degrees and Ph.D.'s in pharmacology, medicine and engineering area. Most of them have translated amount of documents from English, Japanese, German, Korean, French, Russian, Italian and Spanish into Chinese.

4. Medical Device Distribution and Technical Support;

More Until now, we've help some manufac rers' find their exclusive dealer, built sales net work and start sales training work in China.

5. Medical Device Sourcing Business;

To help the domestic manufacturers aboard the overseas market, we act as the bridge to make them build up the business relationship with foreign manufacturers or local distributors.

 
 

    China Pharm Products Registration More>>    Medical Device & IVD Registration More>>

  • Our Services for IDL(Import Drug Licence) of CFDA(sfda)
  • The categories of import drugs in China
  • Requisite documents of Drugs CFDA(sfda)  Registration
  • The drugs which can be exempted from clinical trials in China
  • The procedure for Import Drug CFDA(sfda)  Registration
  • Our Services for IPEL (Import pharmaceutical excipient Licence)
  • Certification Documents need for chemical drugs CFDA(sfda)  Registration
  • the procedure for Import Pharmaceutical Excipient Registration


  • Introduce of China Medical Devices Market
  • Phases and Time of Medical Devices CFDA(sfda)  Registration
  • Which Medical Devices require to Clinical Trial before CFDA(sfda)  approval
  • IVD classified in China
  • IVD (In Vitro Diagnostic) in China
  • CFDA(sfda)  Medical Devices Classification
  • Requisite data of Medical Device CFDA(sfda)  Registration
  • Requisite data of Medical Device CFDA(sfda)  Re-Registration

  •     China Health Food Registration More>>    China Cosmetic Registration More>>

  • Required Documents of Health food CFDA(sfda)  Registration
  • The definition of health food products in China
  • 27 Categories of health functions claims approved by CFDA(sfda)
  • Health Food CFDA(sfda)  Registration Process
  • Requisite data of import Health Food CFDA(sfda)  Registration:
  • Application Form for Registration of Health Food
  • Application Form for New Strain


  • Safety,Applicability and Efficacy Test of Cosmetics
  • How long does the cosmetic test last?
  • Classes of Import Cosmetics in China
  • Import Cosmetic CFDA(sfda)  Registration Procedure
  • Cosmetic CFDA(sfda)  Registration in china
  • Requisite data of import cosmetic CFDA(sfda)  Registration

  •     China CRO Service More>>    China CFDA(sfda)  Regulations More>>

  • CRO Consulting services
  • Non-clinical research Service
  • Clinical Trials in China
  • Medical Documents Translation Service
  • Benefits of INDEPENDENT regulatory representation
  • Main Responsibilities of the CFDA(sfda)
  • Introduce of China CFDA(sfda) 
  • Introduce of RJS Medical Technology Inc.


  • 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 CFDA(sfda)
  • Provisions for Drug Registration

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    | Guangdong:+86-755-25831330 | Beijing:+86-10-51663836 | Shanghai:+86-21-51036093  |

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