Explore all of ul.com

Markets

Asia

China’s Food and Drug Administration (CFDA) has issued Administrative Measures for Drug Standards (Draft).

This draft establishes general formulation, revision, implementation and supervision of drug standards. This draft outlines the following:

  • General principles
  • Programming
  • Formulation and Revision
  • Approval and Promulgation
  • Implementation
  • Review
  • Information Management and Disclosure
  • Supervision
  • Local Drug Standards
  • Supplementary Rules

Source

Share

Subscribe to Newsletter

The CRS monthly Newsletter focuses on the latest initiatives, insights and information for manufacturers and retailers across industries.