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  • A Complete Procedure for DOP Agent working at Agent Portal Yemen price
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  • A Complete Procedure for DOP Agent working at Agent Portal Yemen price
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  • How do I List A distributor in Yemen?
  • Yemeni Agent Name & Address: If applicable, list the name and address of your authorized distributor in Yemen. Therapeutic Category: Specify the therapeutic category or class of medication (e.g., antibiotic, analgesic). Dosage Form: Indicate the form of the product (e.g., tablet, capsule, injection).
  • How to get your products approved in Yemen?
  • Now comes the paperwork for manufacturer registration, the first step towards getting your products approved in Yemen. The Supreme Board of Drugs and Medical Appliances (SBDMA) acts as the gatekeeper, and their goal is to ensure your manufacturing capabilities meet their strict standards for safety and quality.
  • How do I get a GMP certification in Yemen?
  • Achieving a recognized GMP certification, such as WHO GMP, cGMP, US FDA or EMA, is a critical first step. All certifications must be legalized by the Yemeni embassy. You must have a detailed site master file (SMF) outlining your manufacturing facilities, quality control procedures, and personnel qualifications.
  • Why should I partner with a local Yemeni distributor?
  • Agent’s Distribution Agreement: Partnering with a local Yemeni distributor is crucial for successfully marketing and selling your products in the Yemeni market. This agreement outlines the terms and conditions under which your agent will handle the distribution process.
  • How does a distributor agreement work in Yemen?
  • All documents are initially reviewed by the Ministry of Industry and Trade. A card is issued by the Ministry confirming that the Yemeni company is the designated distributor of the manufacturer’s products, as stipulated in the agreement. This applies whether the agreement covers a single product or the manufacturer’s entire product range.
  • How do I register a product in Yemen?
  • Once your company is registered, you can proceed with individual product registration. To register your product, you must submit a detailed dossier to the Yemeni Supreme Board of Drugs and Medical Appliances (SBDMA) and the Ministry of Public Health (MOH). The dossier typically consists of two main sections: