Medicinal Products Act 2011

 

Source: This content is embedded from the official website of the Ministry of Health and Medical Services(www.health.gov.fj)

# Title Download
1 Medicinal Products Act 2011 PDF
Measures / Standards
# Name Type Agency Description Law Valid To Apply To
1 Import Permit Medicinal Products Permit Requirement Fiji Medicines Regulatory Authority (MRA) An application to import a medicinal product must be approved by the Medicinal Products Board before the applicant may import that medicinal product. The Board require that the medicinal products imported into Fiji meet prescribed standards of quality, safety, and efficacy, and that they are imported only by authorized and licensed persons. Medicinal Products Act 2011 06-12-0002 ALL
2 Provisional Registration of Medicinal Products Registration Requirement Fiji Medicines Regulatory Authority (MRA) The Medicinal Products Act 2011 section 29 requires that no person shall import, manufacture, export, store, sell, distribute, transport, offer for sale, expose to sale or advertise any medicinal product which is not registered with the Fiji Medicine Regulatory Authority. The process is a requirement for all licensed importers of medicines in Fiji, including wholesalers and pharmacies, regardless of whether they supply the government or the private sector. Overseas-based suppliers to the Ministry of Health and Medical Services (MOHMS) are not required to undergo provisional registration but must apply for Finished Pharmaceutical Product Prequalification for each product they intend to supply. Medicinal Products Act 2011 08-12-0002 ALL
3 Prequalification of Finished Pharmaceutical Products and their Manufacturers. Registration Requirement Fiji Medicines Regulatory Authority (MRA) 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, Medicinal Products Act 2011 10-12-0002 ALL
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