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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
      • 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
    • We are hiring
    • Request a Quote
  • Blog
  • Black deal
    • Test of Chinese market
    • E-Learning of Chinese testing
    • Test of international registration
    • Test of Brasilian market
    • Test of essential requirement
Easy Comparison

Professional comparison in most important markets of medical device

Comparison bw. CH, US and EU Timeline CH & US Significant product change Essential principle of safety and performance CH & EU
Workshop of Chinese registration

Contact

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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


Chinese  registration

International registration

Training (remote and in-house)

Proposal

Knowlege



Sale (up to 50  %):

Template of registration

On-Demand Workshops



Legal notice


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Message us on WhatsApp
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Newsletter



1 Year MyCompliance E-Learning

E-Learning "MyComplinace"

Learning Chinese regulation and global regulatory affairs


Participation possible any time.


Article:

Top 10 news in China


International market of medical device for Startups,SME


Overseas inspecion starts again



From FDA to Chinese NMPA



Significant changes of medical device in China, EU, MDSAP countries


Meet us in next conference:

raps euro convergence 2025



Global compliance and training

Agile project of global registration of medical device
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All Rights Reserve | Easychinapprov

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