DCGI May Waive Testing Requirement For Cough Syrups Exported To Certain Countries

New Delhi: The Central Drugs Standard Control Organisation (CDSCO) is considering a proposal to waive the need for testing cough syrups for export to certain countries after having received a representation from stakeholders seeking such exemption, official sources said on Tuesday.

In May last year, the Directorate General of Foreign Trade, Department of Commerce, Ministry of Commerce and Industry had made it compulsory for cough syrup manufacturers to get samples of their products tested at specified government laboratories from June 1 before getting permission for outbound shipments.

The direction had come after quality concerns were raised globally over cough syrups exported by Indian firms.

Now, the CDSCO, the apex drugs regulatory authority, is examining a proposal to waive the requirement for testing cough syrups being exported to the US, the UK, Canada, the European Union, Japan, Australia, Singapore, Korea and Switzerland at the prescribed laboratory, the sources said.

Further, if a cough syrup is manufactured in a plant or section approved by the regulatory agencies of these countries for any product, it may also be allowed to be exported to any country without testing at the prescribed laboratory, they said.

While the CDSCO is considering waiving the testing requirement, the sources said that according to the latest data, around 353 of 7,087 batches of cough syrups that were tested were found “not of standard quality” on various parameters, including contamination of toxic diethylene glycol and ethylene glycol.

Related Posts

FDA seizes food stock worth Rs 63.45 crore, suspends 954 licences in two months

The Maharashtra Food and Drug Administration (FDA) seized 3,098.46 tonnes of food stock worth Rs 63.45 crore and suspended 954 food licences during a statewide enforcement drive in the past…

Stents to syringes: Serious harm reports surge, but makers remain unnamed

6-year data disclosed first time by Indian Pharmacopoeia Commission on CIC order The Indian Pharmacopoeia Commission (IPC) has, for the first time, disclosed the number of Serious Adverse Events (SAEs)…

Leave a Reply

Your email address will not be published. Required fields are marked *

You Missed

FDA seizes food stock worth Rs 63.45 crore, suspends 954 licences in two months

FDA seizes food stock worth Rs 63.45 crore, suspends 954 licences in two months

Stents to syringes: Serious harm reports surge, but makers remain unnamed

Stents to syringes: Serious harm reports surge, but makers remain unnamed

NPPA Revises Retail and Ceiling Prices of 35 Drug Formulations; Fixes Prices of 34 New Drugs, Cholecalciferol, Oxaliplatin and Sun Pharma’s Diclofenac Gel

NPPA Revises Retail and Ceiling Prices of 35 Drug Formulations; Fixes Prices of 34 New Drugs, Cholecalciferol, Oxaliplatin and Sun Pharma’s Diclofenac Gel

ED attaches assets, freezes bank account in counterfeit medicines racket; searches five premises in Bengaluru

ED attaches assets, freezes bank account in counterfeit medicines racket; searches five premises in Bengaluru

Hyderabad Startup Working On Personalised Cancer Vaccine: What It Means For Cancer Treatment

Hyderabad Startup Working On Personalised Cancer Vaccine: What It Means For Cancer Treatment

Medicines that cure Us are making Our Environment Sick

Medicines that cure Us are making Our Environment Sick