
To obtain an export permit for medicinal products, exporters must manually complete the application form provided by the Fiji MRA. This form, along with necessary supporting documents such as proof of product registration and details about the intended destination, must be submitted to the Fiji MRA for review. The authority evaluates the application to ensure compliance with both local and international standards. Once the application is approved, the Fiji MRA issues the export permit, which legally authorizes the export of the medicinal product for commercial purposes. Currently, export permits are only issued for controlled medicines, and the process is handled manually. Only licensed wholesalers and pharmacies are eligible to apply for an export permit. This process is governed by the Illicit Drugs and Control Act 2004.
Step 1: Register with FCCC
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To sell or supply medicines to anyone other than the patient using the medicine, you must obtain a wholesaler license. |
Step 2: Prepare the Application
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To apply for the export permit, visit the nearest local health office or email MRA to request a copy of the application, or download the form from FTIP. Complete the application carefully and attach all required documents. |
Step 3: Visit MRA and Submit the Completed Application
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Submit the completed application and required documents via email to Medicine Regulatory Authority or in person at any local health office. The MRA will review the submission, and if any documents are missing or incomplete, you will be notified to provide the necessary details. |
Step 4: Visit MRA and Collect the Export Permit
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Collect the Export license for medicinal products in person at the MRA office. If the application is rejected, the applicant will be notified by email with the reasons for rejection. |
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