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EasyChinapprov           

Agile project of global registration of medical device
  • Home
  • Service
    • Chinese registration
    • International registration
    • Service in Europe
    • Chinese talent pool
    • Interim manager
    • Training and Meeting
    • Legal representative | Agent | Rep
    • Outsourced testing
  • Digital solution
    • Template
      • Working instruction of technical documentation in China
      • Template of Periodic Risk Evaluation Report
      • Example of Chinese label
      • Example of product technical requirements
      • Example of product registration technical review report
      • Electronic Chinese adverse event reporting form
      • Chinese site master file
    • eLearning
      • 1.0 Road map of Chinese registration
    • On-Demand workshops
      • Workshop of Chinese registration
      • Workshop of Chinese technical document
      • Workshop of PTR
      • Workshop of type testing
      • Workshop of design change in China
      • Workshop of intercultrural communicaiton
      • Workshop for international markets
    • Online university
  • Knowledge
    • About Chinese authority NMPA
    • Basic (CN)
      • Encyclopedia of medical device and IVD in China
      • Chinese agent
      • Product code, product classification and type of product registration
      • Time and Cost
      • Chinese Certificate
      • Change registration
      • How to file class I medical device?
      • Electronic Registration System in China
    • Key (CN)
      • NMPA registration procedure in video
      • Chinese technical documentation
      • Product technical requirement
      • Type testing
      • Clinical Evaluation
      • Aging - or stability test
      • Chinese quality management annual report
      • Periodic Risk Evaluation Report
      • Chinese labelling
      • Overseas inspection
    • International
      • International markets for Start-ups
      • Registration in Brazil
      • International requirement of QM
      • Registration in Canada
      • Registration in Vietnam
      • Registration in ASEAN
      • Registration in Taiwan
      • Verification and validation
      • Device Description
      • Essential principle of safety and performance
      • Contract partner
    • Easy Comparison
      • Comparison overview
      • International Legal representative
      • Quality management system
      • From FDA to China
      • From MDR to NMPA
      • Timeline in US and in China
      • Significant product change
    • Q&A
      • Special Q/A for overseas medical device
  • Who we are
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  • Blog
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    • Test of Chinese market
    • E-Learning of Chinese testing
    • Test of international registration
    • Test of Brasilian market
    • Test of essential requirement
CN Classification
Workshop of Chinese registration

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Dear Sir/Madam,

Thank you for contacting us.

We will answer you as soon as possible.


regards,


CEO

Antonio Lee

Easychinapprov

China, Germany

Ups, beim Senden Ihrer Nachrichtes ist ein Fehler aufgetreten.
Bitte versuchen Sie es später noch einmal.

Contact us


Frankfurt, Stuttgart                  Germany


Sun Dong An Plaza, No. 138
Beijing                                China   

info@easychinapprov.com

0049-17638379004


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1 Year MyCompliance E-Learning

E-Learning "MyComplinace"

Learning Chinese and global regulatory affairs of medical device


Participation possible any time.


Article:

Chinese landscape of critical process


International market of medical device for Startups,SME


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Agile project of global registration of medical device
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