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Get the free APPLICATION FOR THE PARALLEL IMPORTATION OF MEDICINAL PRODUCTS

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This document serves as an application form for the parallel importation of medicinal products that already have marketing authorization in Malta. It includes sections for details of the importer,
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How to fill out application for form parallel

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How to fill out APPLICATION FOR THE PARALLEL IMPORTATION OF MEDICINAL PRODUCTS

01
Download the APPLICATION FOR THE PARALLEL IMPORTATION OF MEDICINAL PRODUCTS form from the relevant regulatory authority's website.
02
Fill in the applicant's details, including name, address, and contact information.
03
Provide information about the medicinal product, including its name, active ingredients, and intended use.
04
Include details about the country of origin and the country where the product will be imported to.
05
Attach any required documentation, such as a marketing authorization or proof of compliance with safety standards.
06
Sign and date the application form.
07
Submit the completed application to the designated regulatory authority along with the applicable fees.
08
Keep a copy of the submitted application for your records.

Who needs APPLICATION FOR THE PARALLEL IMPORTATION OF MEDICINAL PRODUCTS?

01
Pharmaceutical companies seeking to import medicinal products not available in their local market.
02
Healthcare providers looking to access specific medications for their patients.
03
Businesses involved in the distribution of pharmaceuticals that require access to imported medicinal products.
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It is a formal request submitted by entities seeking to import medicinal products that are legally marketed in one country to be sold in another, often to facilitate access to medicines at potentially lower prices.
Typically, licensed wholesalers, distributors, or pharmaceutical companies that plan to import medicinal products for commercial sale are required to file this application.
The application must be filled out with specific details about the medicinal product, including its name, dosage form, packaging, marketing authorization in the exporting country, and proof of compliance with safety and efficacy standards.
The purpose is to ensure that imported medicines comply with local regulations while maintaining competitive pricing and availability for consumers.
The application must include product details (e.g., name, dosage), marketing authorization details, the name of the importer, and evidence of compliance with health regulations.
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