Widget Name: blog home
Error Message: structuredClone is not defined
Oops! Something went wrong while rendering the widget.
The cure India's medical devices ecosystem needs
Effective public-private sector collaboration in times of crisis will show the way for a self-reliant medical devices sector
Coronavirus has been a stress-test for every country's health infrastructure. In India, under-investment and pre-existing gaps in demand and supply of high-quality medical infrastructure, and shortage of skilled health workers, has only further exposed the country’s vulnerabilities in managing its mounting health burden.
In the past months, even as India struggled to accommodate and treat critical coronavirus cases, elective procedures in general surgery and specialties including orthopaedics and bariatric were down by over 90 percent. There is emerging evidence that critical care for oncology, cardiovascular and other urgent conditions is being underutilised by over 60 percent, creating unprecedented collateral damage to overall health systems and long-term implications for patients. This lack of access to healthcare when needed has led to a trust deficit among patients and the healthcare system.
India’s well-intended but rapidly changing regulatory guidelines and fiscal policies create uncertainty and further impede the strengthening of our healthcare sector, ultimately impacting our economic growth. It is a good time to reflect on the paradigm shift needed in our health system. To work towards this shared purpose with cohesive planning and collaboration between the government, private sector and multinational companies that are equally invested in India.
Under the Medical Device Rules 2017, voluntary registration is required for all medical devices starting April 1, 2020. Considering the operational difficulties related to COVID-19 and dependency on multiple domestic and foreign bodies for sourcing documentation, the Government should consider extending the current voluntary registration period and subsequent dates by 6-12 months. For Public Procurement Order (PPO), any increase in local content percentage for medical devices should only be done based upon feasibility, and in consultation with the industry, in a phased manner over a period of at least five years, instead of one to three years as envisioned in the PPO. Considering that the regulation of quality management systems (QMS) is in the early stages of development, class C and class D devices should be exempted from the scope of PPO.
India is poised to become the global lab for innovation, leadership and growth. A clear strategy, collaborative approach by medical devices manufacturers, hospitals, scientific bodies, investors and key partners—facilitated by the government, will set India on a self-reliant path to becoming an export powerhouse of high-quality value-based products and services to the world.