The Indian government has made laboratory testing of cough syrups mandatory, prior to their export, officials said yesterday.
According to a notification, issued by the Directorate General of Foreign Trade (DGFT), on Monday evening, an amendment in the export policy of cough syrup has been made.
The revised policy, which will come into effect from June 1, states that, companies will have to get a certificate of analysis from a government-approved laboratory.
“Cough syrup shall be permitted to be exported, subject to the export sample being tested and production of a certificate of analysis,” read the notification.
The amendment has come, after some India-made cough syrups were linked to deaths in The Gambia and Uzbekistan.
Since then many Indian pharma companies have come under the scanner for the quality of their drugs.
Last month, the World Health Organisation (WHO) issued an alert for made-in-India cough syrup – Guaifenesin Syrup TG Syrup – noting it contains “unacceptable amounts of diethylene glycol and ethylene glycol.”
The batch of the contaminated India-made cough syrup was found in the Marshall Islands and Micronesia.
Last Oct, WHO sounded a global alert and linked four cough syrups made by Maiden Pharmaceuticals Limited, India, to the deaths of 66 children from kidney injuries in The Gambia.
In Mar this year, authorities in the northern Indian state of Uttar Pradesh, cancelled the manufacturing licence of the pharmaceutical firm, Marion Biotech, whose cough syrup Doc-1 Max, was alleged to have caused the death of 18 children in Uzbekistan.
In another development, the U.S. Food and Drug Administration said, India-made eye drops were linked to at least three deaths and a deadly outbreak of drug-resistant infections in the United States.
Source: Nam News Network (NNN)