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Reporting adverse events of medical products from medical companies

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Service completion duration

  • 10 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
10 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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