Alpha is a Department of Health & ACTVET Approved, ISO 9001:2015 Certified Healthcare Management Consultancy

Medical Devices & Pharmaceutical
Product Registration in UAE

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UAE is an attractive marketplace for existing and potential pharmaceuticals to set up and flourish due to its reputation of high Medical Standards, increasing health conscious lifestyles and growing popularity globally as a desirable destination for Medical Tourism with its world class Medical facilities, relatedly much more affordable than other developed nations. While the registration process and legislations are meticulous and lengthy , the purpose is to maintain distinct standards that guarantee safety and wellness of consumers.
It is beneficial to recruit an experienced process experts as we are the one-stop solution for entire pharmaceutical importers and manufacturers to introduce your product to the global market through UAE in terms of setting up a Drug store or pharmaceutical import license, product classification & registration. We can cover the entire process in detail as assist with all matters from the initial stage to completion of successfully setting up.

Alpha health consultancy will answer all registration related queries, explain the process and help with all technicalities. We also take responsibility to monitor the whole process once the registration applications are submitted till the certification is done and furthermore will assist with other related services too.

Ministry of Health and Prevention (MOHAP) of UAE regulates the import and distribution of conventional, biological or other human pharmaceutical products by the Importers and manufacturers of pharmaceutical products, therefore it is mandatory to register with MOHAP to sell any products anywhere in the UAE.We handle the full process from registration & classification through the Ministry of Health services.

Product Import Process in UAE

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We handle all medical product classification & registration processe with MOHAP and get it ready for you to clear your shipment in UAE. Our medical product specialists handle all the technicality & responsibility to deliver the whole process.



Documents Requirements

The entire product related documents only then the official fee has to be submitted along with the application. The application is first checked by the Technical team before forwarded to the Ministerial Committee for final decision. Further follow up needs to be carried out from a Pharmacological Analysis Section of at the Drug Department and other requirements have to be submitted through E-services. Once the Technical committee has a thorough examination of the products again and approves registration.

  • Trade License & Drugstore License
  • Product Catalogue for Medical Devices
  • Product Technical Sheet
  • Authorization Letter
  • Certificate from the Authorities in the Country of Origin
  • Leaflet/Product Information in English/ Arabic.
  • Inner Pack Label with Product Information
  • Outer Pack Label Product Information
  • Composition Certificate /MSDS

Frequently Asked Questions

We have listed the very frequent questions here, you may have some more, please don’t hesitate to leave us a message with your own question, our team is ready to answer your query

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