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Why you should buy this report

This report is a single point solution to study end-to-end regulations imposed on In-vitro Diagnostic Device (IVD) in Cote d’Ivoire.

The objective of this report is to provide precise information on the Regulatory landscape of Cote d’Ivoire, so as to enable a Regulatory go-to-market strategy and ensure compliance.

Summary
  • Provides information on product definition and their governing regulations;
  • Carefully explains the information on IVD registration process;
  • Precise information on health authority fees, timelines for registration, submission modes (online/in person) and validity;
  • Additional information on of the registration, renewal process;
  • Details the regulations applicable on labeling;
  • Describes the information on import regulations; and
  • Explains the bidding/tender regulation set by Cote d’Ivoire government with minutes discussion with eligibility and qualification required for tenderer.
Table of Contents
  1. LIST OF ABBREVIATIONS
  2. GOVERNING BODY AND REGULATIONS
  3. DEFINITION
  4. PRODUCT REGISTRATION
    1. Wholesale Dealer Registration.

      1. Process
      2. Required Documentation
      3. Submission Mode
      4. Fee.
      5. Validity of the Registration Certificate
  5. IMPORT PERMIT
    1. Process
    2. Required Documentation
    3. Timeline
  6. RENEWAL 2
    1. Process.
    2. Required Documentation
    3. Fee
  7. LABELING
  8. GOVERNMENT TENDERS
  9. CONCLUSION
  10. REFERENCES
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