Applications for the supply of medicinal products to Fiji must be submitted through the Fiji MRA Online Services Portal. Suppliers are required to comply with internationally recognized pharmacopeial standards, such as the BP, Ph. Eur.., Ph. Int., and USP. Additionally, suppliers must be registered, and manufacturers must hold valid Good Manufacturing Practices (GMP) certification from a recognized National Regulatory Authority (NRA). Finished pharmaceutical products must adhere to strict labelling and packaging standards and must be identical to those registered in the country of origin. The prequalification process is mandatory for all medicines intended for procurement or use by the Ministry of Health and Medical Services through the Fiji Pharmaceutical and Biomedical Services (FPBS). Both local and overseas-based suppliers must have their products prequalified before they can be purchased for use in Fiji.
Step 1: Create an Account with Fiji MRA Online Service Portal [Online]
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Applicants are to visit the Fiji MRA Online Services Portal to create a user account using the online registration form and register. |
Step 2: Submit Your Application [Online]
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To apply for an import permit for medicinal products in Fiji, applicants must use the Fiji MRA Online Services Portal, which is accessible via the Fiji MRA website. The process involves registering an account on the Portal, where applicants can submit their application for approval. |
Step 3: Obtain Prequalification of Finished Pharmaceutical Products [Online]
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The Board must approve an application for the Prequalification of Finished Pharmaceutical Products before they can be supplied to the Fiji MHMS |
| # | Title | Description | Issued By | File |
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| # | Name | Description | Measure Type | Agency | Comments | Legal Document | Validity To | Measure Class |
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| 1 | Prequalification of Finished Pharmaceutical Products and their Manufacturers. | Prequalification of Finished Pharmaceutical Products (FPPs) and Their Manufacturers are based on the National Medicinal Products Policy 2013 and the Medicinal Products Act 2011. The prequalification process is mandatory for all medicines intended for procurement or use by the Ministry of Health and Medical Services through the Fiji Pharmaceutical and Biomedical Services (FPBS). Both local and overseas-based suppliers must have their products prequalified before they can be purchased for use in Fiji, | Registration Requirement | Fiji Medicines Regulatory Authority (MRA) | Prequalification does not guarantee solicitation for supply, and the Fiji MRA reserves the right to modify application requirements at any stage. | Medicinal Products Act 2011 | 0002-12-08 | Good |
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