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China regulators formalize procedures for medical device expert panel meetings

May 15, 2017 By Danielle Kirsh

Chinese flag medical robotics

By Stewart Eisenhart, Emergo Group

Regulators at the China Food and Drug Administration (CFDA) have published formal procedures for expert panel meetings held to discuss medical device registration issues, clarifying the process for Chinese market applicants.

Get the full story here at the Emergo Group’s blog.

The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MedicalDesignandOutsourcing.com or its employees.

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  • Home
  • Medical Device Business
    • Mergers & Acquisitions
    • Financial
    • Regulatory
  • Applications
    • Cardiovascular
    • Devices
    • Imaging
    • Implantables
    • Medical Equipment
    • Orthopedic
    • Surgical
  • Technologies
    • Contract Manufacturing
    • Components
    • Electronics
    • Extrusions
    • Materials
    • Motion Control
    • Prototyping
    • Pumps
    • Tubing
  • Med Tech Resources
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    • Digital Editions
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    • MedTech 100 Index
    • Podcasts
    • Print Subscription
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    • Video
  • 2022 Leadership in MedTech
    • 2022 Leadership Voting!
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