Is the interim bilateral trade agreement between India and the US a game changer for the health industry?
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New Delhi, Feb 7 (NationPress) Leaders in the health sector expressed their approval on Saturday regarding the interim agreement concerning the bilateral trade arrangement between India and the United States.
Under this interim framework, the US will reduce reciprocal tariffs on Indian products to 18 percent. Additionally, the US will eliminate tariffs on generic pharmaceuticals, as well as other sectors including gems and diamonds, and aircraft components.
While complete details are still forthcoming, the interim trade deal framework suggests that India has secured the “best deal” from the United States compared to its neighboring countries.
“The Association of Indian Medical Devices (AiMeD) welcomes the US-India joint statement addressing trade barriers. It’s important to note that the Central Drugs Standard Control Organization (CDSCO) import licenses for devices from the US are already processed more quickly than those for Indian manufacturers, who face mandatory inspections unlike foreign firms,” stated Rajiv Nath, Forum Coordinator of AiMeD.
He further noted, “The US leads imports at Rs 14,000 crore (20 percent share), outpacing China’s Rs 12,000 crore, with our US exports at $750 million compared to $1.6 billion in imports last year. The US FDA shows a preference for ACSA over NABL labs, creating an imbalance. Indian medtech faces challenges from Chinese WANA dumping, EU CE delays, Japan's yen fluctuations, and biases in Indonesia, coupled with CDSCO hurdles. We call for reciprocal fairness to ensure that trade benefits both nations' innovative capacities,” he added.
Moreover, the agreement states that India will also gain negotiated outcomes concerning generic pharmaceuticals and ingredients based on the findings from the US Section 232 investigation.
“Enhancing the India-US medicines partnership is crucial, as medicine security is intertwined with national security. Generics are exempt from tariffs, and as outlined in the joint statement, all pharmaceuticals (including generics) are currently under US Section 232 investigation. This aligns with the approach taken in various Free Trade Agreements (FTAs),” added Sudarshan Jain, Secretary General of the Indian Pharmaceutical Alliance.