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An insider’s look at the healthcare market in India

The latest on India’s pharmaceutical and medical device markets, with a perspective from Vimal Kumar, Senior Specialist and Head Solutions/Medical Electronics for Tata Elxsi, a design engineering service provider in Pune, India.

Map of India
Map of India

As one of the “big four” or BRIC (Brazil, Russia, India, and China) countries, India is seen as a growing economic power in the developing world.

Similar to other nations, however, India faces its share of challenges. In the pharmaceutical market, for example, an Oct. 31, 2013 report pointed out, “The Indian pharmaceutical market (IPM) is currently valued at 72,069 crore INR as against 65,654 crore INR (Indian Rupees) in 2012. Though the market value has seen an increase, the sector overall has experienced a slowdown with its growth going down to 9.8% from 16.6% in 2012. This slowdown can be attributed to the new drug pricing policy and the regulatory interventions over the last year.” That’s according to the Confederation of Indian Industry (CII) and PricewaterhouseCoopers (PwC) report, “India Pharma Inc; Changing Landscape of Indian Pharma Industry.”

That report noted, “The industry is witnessing additional challenges like delays in clinical trial approvals, uncertainties over the FDI policy, a uniform code for sales and marketing practices and compulsory licensing. The slowdown is also evident from the number of new product launches, which has gone down from approximately 1900 in year 2010 to 1700 in year 2012.”

According to the report, “India is perceived as an attractive destination for clinical trials but has been marred with genuine concerns. Clinical trials are an inherent part of the drug development process and cannot be dispensed with. The continuing search for new therapies and cost-effective alternatives to existing therapies will be realized in practice only after comprehensive clinical trials.

“The clinical research industry in India needs to work closely with the government to create a regulatory mechanism that allows scientifically sound and ethically correct trials to be conducted so that the benefits of clinical trials can be brought to patients in India.

“The industry is also facing stricter regulations on manufacturing and quality practices in the domestic as well as he international markets. Indian companies will have to raise their compliance to U.S. FDA regulations as they drive their major share of exports from the US market.”

Healthcare Packaging asked Vimal Kumar, Senior Specialist and Head Solutions/Medical Electronics for Tata Elxsi, to describe the economic climate in India and what impact that has on the development of pharmaceuticals, biologics, and medical devices.

“While China is the manufacturing hub, India is a design hub,” said Kumar, whose company Tata Elxsi, is a design engineering service providerof design and innovation, R&D, and product engineering services to medical equipment manufacturers. Tata Elxsi serves market segments that include diagnostics, drug delivery, renal care, cardiology, orthopedics, diabetes care, endoscopy, surgical, point of care, infusion pump, critical care, therapeutics, and IVD devices.

INTRODUCING! The Latest Trends for Life Sciences at PACK EXPO Southeast
The exciting new PACK EXPO Southeast 2025 unites all vertical markets in one dynamic hub, generating more innovative answers to packaging challenges for life sciences products. Don’t miss this extraordinary opportunity for your business!
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INTRODUCING! The Latest Trends for Life Sciences at PACK EXPO Southeast