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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 Zimbabwe. Its highly diversified industrial base provides the investor with a number of opportunities.

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

Summary
  • Provides information on product definition and governing regulations;
  • Precise information on product registration;
  • Describes the information on import regulations and local agent requirements;
  • Precise information on import application documentation, fees and validity of import authorization;
  • Details the regulations applicable on labeling; and
  • Explains the bidding/tender regulation set by Zimbabwe government with minutes discussion with eligibility and qualification required for tenderer.
Table of Contents
  1. LIST OF ABBREVIATIONS
  2. GOVERNING BODY & GOVERNING REGULATION
  3. DEFINITION
    1. Categorization of the Product Groupings
  4. CLASSIFICATION
  5. PRODUCT REGISTRATION
  6. IMPORT PERMIT 2
    1. Process

      1. Issue of Permit
      2. Consignment Verification
      3. Preservation of Records
      4. Ports of Entry
    2. Documents Required
    3. Fee
    4. Timeline
    5. Validity
  7. LOCAL AGENT REQUIREMENTS 4.
    1. Qualification of Authorised Person
    2. Responsibilities of an Authorised Person 4
  8. LABELING
  9. GOVERNMENT TENDERS
    1. Eligibility of Suppliers
  10. CONCLUSION
  11. REFERENCES
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