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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 Angola. As Angola relies primarily on imported medical equipment, devices, supplies and consumables to meet local demand, it offers realistic options for a business.

The objective of this report is to provide precise information on the Regulatory landscape of Angola, 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;
  • Precise information on import application documentation, fees and timelines delivery mode of import authorization;
  • Details the regulations applicable on labeling; and
  • Explains the bidding/tender regulation set by Angolan government with minutes discussion with eligibility and qualification required for tenderer.
Table of Contents
  1. LIST OF ABBREVIATIONS
  2. GOVERNING BODY & REGULATIONS
  3. DEFINITION
  4. CLASSIFICATION
  5. PRODUCT REGISTRATION
  6. IMPORT PERMIT 
    1. Process.
    2. Documentation Required
    3. Fee
    4. Timeline
    5. Submission/ Delivery Mode
  7. LABELING
  8. GOVERNMENT TENDERS
    1. Eligibility
  9. CONCLUSION
  10. REFERENCES
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