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Why you should buy this report

This comprehensive report provides precise information on the regulations applicable to Medical devices in Morocco, to enable a Regulatory go-to-market strategy and ensure compliance. Morocco is an emerging market for medical devices, and the country’s healthcare sector has been growing rapidly and is open to opportunities for future investment.

 

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.
Table of Contents
  1. LIST OF ABBREVIATIONS
  2. DEFINITION
  3. GOVERNING BODY
  4. GOVERNING REGULATIONS
  5. PRODUCT REGISTRATION
    1. Process
    2. Documents Required for a Locally Manufactured Product
    3. Documents Required for an Imported Product
    4. Fee and Timeline
  6. IMPORT PERMIT
    1. Documentation
    2. Fee and Timeline
  7. VALIDITY AND RENEWAL
    1. Documentation
    2. Fee and Timeline
  8. VARIATIONS
    1. Documentation
    2. Fee and Timeline
  9. QUALIFICATIONS AND RESPONSIBILITIES OF A LOCAL AGENT
  10. LABELLING
  11. REFERENCES
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