India wants China to allow import of drugs cleared by US, Europe

NEW DELHI: India has requested China to allow imports of Indian drugs cleared by the drug administrators of the United States, European Union and Japan, as China recognises these approvals. It has also sought a special price category for Indian generics so that they don’t compete with branded products.

Almost 1,500 Indian products have obtained clearances from the food and pharmaceutical regulators of the US, EU and Japan, but only 535 are registered with China and can be sold there.

“Our pharma export to China is a pittance. We have requested if China FDA (food and drug administration) could give suo motu registration to companies cleared by the US, EU and Japan because it recognises these,” an official told ET on condition of anonymity. “We want our generics in a special price category so that we don’t get into competition with branded products.”

Though India is the world’s largest supplier of generic medicines, with 20-22% share of global exports, it exported pharma products worth a meagre $41.07 million to China in 2017-18 and only $26.1 million in the first half of the current financial year. Commerce department officials have said that India’s share in China’s pharma imports is merely 1%.

Another issue that India has raised with China pertains to multiplicity of approvals as every Chinese province has different prices and rules for pharmaceutical imports.

India has, therefore, also sought a waiver of local provincial approvals for Chinese companies which import Indian generic injectable drugs. The provincial clearance is required even after the CFDA nod.

The move is aimed at increasing exports of pharmaceuticals to China and reduce the trade deficit. India’s exports to China amounted to $33 billion in 2017-18 while imports from the country were more than double that at $76.2 billion. Indian industry has cited non-tariff barriers such as complicated procedures that hinder pharma exports to China. “We have requested again for familiarity of forms. We need clarity and handholding because their process is long, tedious and cumbersome,” the official said.

  • 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