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About this 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

  • Applicant submits report by email to.

  • MOHAP staff concerned review the report.

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

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

Required documents

  • Report must satisfy all required data.

Conditions and requirements

  • The report should list all required patient data.

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

  • The report should define the required drug data.

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

Service completion duration

3 working days

Service fees

  • Free

SDGs Goals

Service locations

Email: PV@mohap.gov.ae

Support

PV@mohap.gov.ae

Payment channels

  • E-payment

Target audience

  • Marketing offices

  • Medical stores

  • Local and international pharmaceutical factories

  • Patients

  • Health care practitioners

  • Health institutions

Resources

Service category

Business services

Sub service category

Pharmaceutical enterprises services

Main service

Pharmaceutical vigilance

Service code

110-45-003-000

Service classification

  • Government to business

Service type

Transactional

Sub service type

Variation

Number of transactions

0

Notes

This service accepts documents authenticated with the UAE PASS Digital Seal.

Start service

Service completion duration

3 working days

Service fees

  • Free

Average rating

0 From 0 Users

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