Rule to Import Quality Medicines from Europe Being Reviewed

The Maldives Food and Drug Authority (MFDA) has initiated a comprehensive review of its regulations to ensure the importation of high-quality medicines from Europe, according to statements by Health Minister Abdulla Khaleel. 

Speaking to Mihaaru on Monday, the minister emphasised the collective desire of all stakeholders to facilitate the importation of superior pharmaceuticals. However, challenges to existing rules have prompted the agency to consider modifications, with an official announcement of changes anticipated in the near future.

advertisement

advertisement

advertisement

Khaleel highlighted a potential revision in drug regulations, suggesting that drugs manufactured in European countries could be imported to the Maldives if approved by the respective government. 

The minister acknowledged a key hurdle faced by the Maldives—the necessity to provide detailed drug content information when applying for a license. He expressed concern over the opacity maintained by large pharmaceutical companies regarding the manufacturing details of their drugs.