Centre proposes 10 new entry points for drug imports into India, Noida airport included

The Centre has proposed expanding India's authorised import network for pharmaceuticals and medical devices by adding ten new locations. These include Noida International Airport and several inland container depots across industrial hubs in India....

Agencies

Centre proposes 10 new locations, including Noida International Airport, for importing medicines and medical devices into India.

Imported medicines and medical devices could soon have more entry points into India, with the Centre proposing to add 10 locations to the country's authorised import network, including Noida International Airport and several inland container depots across key industrial hubs, TOI reports.

The proposed expansion is expected to make it easier for companies to bring healthcare products into the country and clear consignments closer to their warehouses, manufacturing units and distribution centres, potentially reducing transportation costs and delays.

Under a draft amendment to Drugs Rules, 1945, the health ministry has proposed adding ICDs at Sonipat, Piyala and Harsaru in Haryana; Dadri in Uttar Pradesh; Gandhidham/Mundra in Gujarat; Sanath Nagar and Thimmapur in Hyderabad; and Whitefield in Bengaluru. The Bommasandra Special Economic Zone in Karnataka has also been proposed as an entry point.


Noida International Airport has been proposed specifically for the import of drugs by air.

The proposed locations will supplement the existing authorised network, which includes ICDs at Dhannad and Tihi in Indore, along with notified airports and other entry points.

At present, Rule specifies the ports, airports, railway stations, road crossings and other locations through which drugs can be imported into India. The proposed changes seek to widen this network to facilitate the movement and clearance of drugs, medical devices and cosmetics.
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The ministry has invited objections and suggestions on the draft amendment before finalising the changes. Responses can be sent to the Under Secretary (Drugs Regulation), Ministry of Health and Family Welfare.

(With inputs from TOI)
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