Global Star Rating System for Services
Menu
Search

Amend the Registration Data of a Medical Company or a Manufacturer Licensed to Market

Start Service
Bookmark service

Service completion duration

  • 10 working days
View more

Service fees

  • Certificate of amendment to any registration data ...
View more
Export as
Export as  PDF
Export as  XLS

Service Rating

Average Rating : From 0 users

About the Service

This service enables medical companies and manufacturers to submit their applications to amend their registration data.

Service Process

  • 1
    Login to the MoHAP website or smart app using the UAE PASS

    • 2
      Submit the request online, meet all conditions and pay the required fees

      • 3
        The competent technical committees will examine the file and refer it to the competent ministerial committee

        • 4
          Letters are to be addressed to the concerned companies stating the committee's decisions

          • 5
            The customer will follow up with the Pharmacological Analysis Section of at the Drug Control Department

            • 6
              The company should complete the requirements and submit them via electronic service

              • 7
                The relevant technical and ministerial committees will re-deliberate the registration of products that have been deferred in advance as soon as companies complete the requirements

                • 8
                  The certificates of minor changes will be issued after fulfilling all conditions and requirements approved by MOHAP

                  Conditions & Requirements

                  1. The applicant must be a medical warehouse licensed by MOHAP and must hold a valid license.

                  2. The Company must provide the valid approval of the competent authorities in the country of origin regarding such submitted changes.

                  FAQ’s

                  1. What are the fees for the issuance of an amendment certificate concerning any registration date of a medical company or a manufacturer holding the marketing rights?
                    Amendment certificate concerning any registration date of a medical company or a manufacturer holding the marketing rights: AED2,000.
                  2. What is the average length of time for the issuance of an amendment certificate concerning any registration date of a medical company or a manufacturer holding the marketing rights?
                    10 working days.
                  3. What channels are available to apply for the issuance of an amendment certificate concerning any registration date of a medical company or a manufacturer holding the marketing rights?
                    MOHAP Website and Smart Application.
                  Service completion duration
                  10 working days
                  Service fees

                  Certificate of amendment to any registration data of a medical company or a manufacturer with marketing rights: 2000 AED

                  Service channels
                  • MOHAP Website

                  • MOHAP Mobile App

                  Payment channels
                  • E- Payment

                  Target audience
                  • Medical warehouses

                  • Local Pharmaceutical manufacturers

                  • Marketing offices

                  Department name

                  Drug

                  Sector name

                  Health Regulation

                  Main service

                  Medical, Pharmaceutical and Drug Licencing and Registration

                  Service Code

                  110-04-009-000

                  Service Classfication

                  Transactional

                  Service Type

                  Government to Business

                  Sub Service Type

                  Variation

                  Related Services
                  • This service is not linked with other services

                  Service Bundle

                  This service is not linked with any service packages

                  Number of Users

                  14

                  Number of Transactions

                  78

                  Notes

                  The valid electronic seal is accepted for documents of government entities and companies.

                  Required Documents
                  • A legalized letter issued by the company on its original letterhead, signed and stamped by the responsible person in the company, authorizing a person or a local establishment to submit the registration file on its behalf, to the Drug Control Department. Attested true by UAE Embassy. This person / the local establishment will be responsible to receive the registration certificate from the Drug Control Department

                  • Legalized Current GMP Certificate Issued By The Competent Authority In Country Of origin. (Attested True By The UAE Embassy In country of origin).

                  • Legalized Valid Manufacturing License Issued By The Competent Authority In Country Of Origin. (Attested True By the UAE Embassy In country of origin).

                  • List of medicines manufactured at the manufacturing site.

                  • Site Master File

                  • Certified copies of certificates of registration/ certificates of good manufacturing practice of the manufacturing site in other countries.

                  • A Declaration Letter Issued By The Company On Its Original Letterhead, Signed And Stamped By The Responsible Person In The Company , Showing The Details Of Minor Change With Existing Details & Proposed Minor Changes.

                  • Current Registration Certificate Issued By MOHAP UAE.

                  Sustainable Goals
                  Good Health And Well-Being

                  Did you find the content useful ?

                  Give us your feedback so we can improve your experience


                  Yes No

                  Help us improve MOHAP website

                  Give us your feedback so we can improve your experience

                  Thank you for your feedback.