• AZAZ
  • RURU
AEM
+994 12 596 05 20
Write us
No Result
View All Result
  • About Us
  • Import
    • Documents
    • Letter samples
  • Control
    • Control on Medicines
    • Legislation
  • Registration
    • Department of Registration
    • Legislation
  • Laboratory
    • About the Quality Control Laboratory
  • Pharmacovigilance
    • General information
    • Legislation
    • Information for healthcare professionals
    • Information for Patients
    • Pharmacovigilance dictionary
    • Reporting forms
    • Online reporting
    • For MAH
    • Medicines under additional monitoring
  • Private medical institutions
    • Legislation
  • FS
    • Expertise of FS
    • Result of the Expertise of FS
  • Medical devices
    • Application form
    • MD Documents
    • Results of examination of medical devices
    • Legislation
  • MD monitoring
    • Tracking and Tracing of Medicines Department
AEM
No Result
View All Result

Cough syrups recognized by WHO as substandard are not registered in Azerbaijan

October 6, 2022
A A

The World Health Organization (WHO) has issued an alert to national pharmaceutical regulators around the world regarding 4 cough and cold syrups manufactured by the Indian company Maiden Pharmaceuticals. According to the October 6, WHO medical product alert, Promethazine Oral Solution BP, Kofexmalin Baby Cough Syrup, Makoff Baby Cough Syrup, Magrip N Cold Syrup are substandard medical products. Substandard medical products are products that fail to meet either their quality standards or specifications. It should be noted that according to the registration database of Registration and Expertise Department of Analytical Expertise Center, the mentioned medical products are not registered in the territory of the Republic of Azerbaijan.

ShareTweetShare
AEM

© 2022 AEM - Analitik Ekspertiza Mərkəzi .

Useful links

  • About Us
  • Contact
  • Rates

Follow us

  • AZAZ
  • RURU
No Result
View All Result
  • About Us
  • Import
    • Documents
    • Letter samples
  • Control
    • Control on Medicines
    • Legislation
  • Registration
    • Department of Registration
    • Legislation
  • Laboratory
    • About the Quality Control Laboratory
  • Pharmacovigilance
    • General information
    • Legislation
    • Information for healthcare professionals
    • Information for Patients
    • Pharmacovigilance dictionary
    • Reporting forms
    • Online reporting
    • Contacts
    • For MAH
    • Medicines under additional monitoring
  • Private medical institutions
    • Legislation
  • FS
    • Expertise of FS
    • Result of the Expertise of FS
  • Medical devices
    • Application form
    • MD Documents
    • Results of examination of medical devices
    • Legislation
  • Rates
  • Contact

© 2022 AEM - Analitik Ekspertiza Mərkəzi .

Accessibility

Content Scaling
Default
Text Magnifier
Dyslexia Friendly
Highlight Links
Font Sizing
Default
Left Aligned
Center Aligned
Right Aligned
Dark Contrast
Monochrome
High Saturation
Adjust Text Colors
Adjust Title Colors
Adjust Background Colors
Hide Images
Reading Guide
Reading Mask
Highlight Hover
Big Dark Cursor
Big Light Cursor