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China Reshuffles the China Food and Drug Administration (CFDA)

In March 2018, China’s National People’s Congress approved plans for the China Food and Drug Administration (CFDA) to be merged into a newly formed National Market Supervision Administration, part of an overhaul of ministries. The government also plans to set up a new bureau to consolidate the administration of national health insurance and social security funds.

The draft would mean the State Council will be composed of 26 ministries and commissions. Furthermore, the changes will mean that the CFDA will no longer be a standalone department but will be part of a larger unit.

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  • Industry Reports
  • Understanding the Translation Requirements of the EU CTR
  • China Reshuffles the China Food and Drug Administration (CFDA)
  • Understanding the New IVDR
  • Why Medical Translation is a Critical Outsourced Service
  • While We Wait: The EU Joint Plan for Immediate Actions
  • The New China: Medical Device Regulatory Overhaul
  • How are the European Union Medical Device and IVD Regulations Evolving?
  • The Debate Over Changing the EU Medical Device Law
  • India’s Medical Device Market and Regulatory Landscape
  • Requirements for E-Labeling
  • ISO 14155:2011: A First Look
  • Labeling Impact on Worldwide Market Clearance
  • Directive 2007/47/EC
  • European Translation Requirements and Trends for Medical Devices and Pharmaceuticals
  • Helpful Guidelines to Choosing Your Medical Translation Partner
  • More Guidelines to Choosing Your Medical Translation Partner
  • Asian Translation Requirements – Directive 2007/47EC
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