Why you should buy this report

This report is a single point solution to study end-to-end regulations imposed on traditional medicines in Kazakhstan, where traditional medicines have become more popular due to the higher awareness amongst the consumers about health and wellness.

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

Summary

• Underlines the regulations that govern traditional medicines in Vietnam;
• Provides information on product registration, applicable fees and timeline;
• Outlines the submission mode of dossier;
• Provides information on validity, renewal and variations;
• Furnishes the regulations of import that are levied on traditional medicines;
• Includes precise information on the qualification and responsibilities of a legal representative;
• Provides information on the list of ingredients which are approved and restricted from use in traditional medicines;
• Details the regulations imposed on labeling of traditional medicines;
• Includes information on quality and safety that should be maintained while handling traditional medicines;
• Furnishes the regulations on advertising traditional medicines; and
• Provides information on warehousing requirements for traditional medicines.

Table of Contents

1. GOVERNING BODY
2. DEFINITION
3. GOVERNING REGULATIONS       
4. PRODUCT REGISTRATION
   1. Documents Required
   2. Submission Mode
   3. Fee & Timeline
   4. Validity
   5. Renewal
   6. Registration Process
5. IMPORT
   1. Import Process
   2. Documents for Import Permit
   3. Fee and Timeline
   4. Company Registration
      1. Registration of LLP or a Branch
      2. Registration as an Individual Entrepreneur
6. VARIATIONS
   1. Documents for Variation Application
   2. Process of Variation Application
   3. Fee and Timeline
7. LOCAL AGENT REQUIREMENTS
   1. Qualifications of an Importer/ Distributor
   2. Responsibilities of an Importer/ Distributor
   3. Qualification and Responsibilities of a Sanitary Responsible person
8. INGREDIENTS
   1. Permitted and Prohibited Ingredients
   2. New Ingredient Registration
9. CONTAMINANTS
10. QUALITY AND SAFETY
11. SAMPLES FOR ANALYSIS
12. LABELING
13. ADVERTISING
14. CLAIMS
15. WAREHOUSING
16. REFERENCES

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