Medical Device Regulation Report, Morocco, Registration

This report provides information on regulations imposed on medical device in Morocco for product registration, import permit, validity & renewal process, variations filing, legal representative and labeling.
Summary
  • Product definition and governing regulations;
  • Information on medical device registration;
  • Explains the process of registration through flowcharts;
  • Precise information on health authority fees & timelines for registration;
  • Additional information on the validity of registration, renewal process and variation filing
  • Presents the regulations applicable on labeling; and
  • Describes the information on import regulations, and the requirement of a legal representative.

Check out more details at Medical Device Regulation Report, Morocco, Registration

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