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Reporting adverse events of medical products from medical companies

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Service completion duration

  • 3 working days

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Service fees

  • Free
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Service Rating

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About the Service

This service enables companies to request the evaluation of mandatory reports on the side effects and adverse reactions to local and internationally manufactured medicines imported into the UAE.

Service Process

  • 1
    Applicant submits report by email to.

    • 2
      MOHAP staff concerned review the report.

      • 3
        Report is then sent to the World Health Organization (Uppsala Monitoring Center).

        • 4
          If necessary, circulars will be issued regarding the report.

          Conditions & Requirements

          1. The report should list all required patient data.

          2. The report should state all required data of the writer.

          3. The report should define the required drug data.

          4. The report should clearly state the side effects experienced from the drug.

          Service completion duration

          3 working days

          Service fees

          Free

          Service channels
          • MOHAP Website

          Payment channels
          • E- Payment

          Target audience
          • Marketing offices

          • Medical stores

          • Local and international pharmaceutical factories

          • Patients

          • Health care practitioners

          • Health institutions

          Department name

          Drug

          Sector name

          Health Regulation

          Main service

          Pharmaceutical vigilance

          Service Code

          110-45-003-000

          Service Classfication

          Transactional

          Service Type

          Government to Business

          Sub Service Type

          Variation

          Required Documents
          • Report must satisfy all required data.

          Sustainable Goals
          Good Health And Well-Being

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