National Medical Devices Policy, 2023 Approved by the Union Cabinet
The medical devices industry in India is a rapidly expanding sector that shows great potential. It is estimated that the market size of the medical devices sector in India reached $11 billion (approximately ₹ 90,000 Cr) in 2020. This accounts for around 1.5% of the global medical device market ( 1 ✔ ✔ Trusted Source
The Gazette of India
National Medical Devices Policy, 2023 Approved by the Union Cabinet
The National Medical Devices Policy 2023 approved is aimed to create measures to accelerate the orderly growth of the medical device sector.
‘“The National Medical Devices Policy (NMDP) revolutionizes the Indian medical technology industry and brings innovation to the table”’
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The Need for a NMDP
The growth of the medical device sector in India can be attributed to several factors, including the increasing and aging population, rising per capital and disposable income, growing demand for healthcare infrastructure, the emergence of diagnostic services, and the availability and expansion of healthcare services and insurance.
The medical device sector has immense potential to contribute to public health objectives by ensuring the availability of quality products. Therefore, there is an urgent need for a comprehensive policy that accelerates the growth of this sector and harnesses its full potential. While the government has implemented various schemes and programs through different departments to promote the medical devices sector, there is a necessity to establish a holistic and coordinated framework supported by strategic guidance to ensure sustained growth and development.
To meet the goals of accessibility, affordability, quality, and innovation in public health, it is crucial to facilitate the well-organized expansion of the medical device sector. This requires building a supportive ecosystem for manufacturing, with a strong emphasis on innovation, as well as establishing a robust and streamlined regulatory framework. The policy should also focus on providing support through training and capacity-building programs, along with promoting higher education to cultivate skilled resources aligned with the industry's requirements. Encouraging domestic investments and local production of medical devices aligns with the government's "Atmanirbhar Bharat" (self-reliant India) and "Make in India" initiatives.
The envisioned policy aims to provide the necessary support and guidance to strengthen the medical devices industry, transforming it into a competitive, self-reliant, resilient, and innovative sector that not only meets the healthcare needs of India but also contributes to global healthcare requirements.
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National Medical Devices Policy
- Advocating for universal access to quality medical devices to ensure healthcare services for all
- Enhancing domestic manufacturing capabilities to make devices more affordable and reduce overall healthcare costs
- Emphasizing the importance of quality in domestically manufactured devices to enhance competitiveness
- Improving patient care and outcomes through early diagnosis and accurate treatment
- Promoting preventive and promotive health measures through the widespread use of medical devices
- Ensuring the security of medical devices through local manufacturing capabilities and resilient supply chains
- Fostering research and innovation for technology-driven devices and precision care
- Facilitating the development of skilled manpower aligned with the evolving nature of medical device technologies
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What will the Policy Achieve?
According to the Gazette notification, the NDMP has a set of strategies that will cover six broad areas of interventions. These areas have been identified based on the current challenges facing the sector and the opportunities that lie ahead for fulfilling the sector's potential. These are ( 2 ✔ ✔ Trusted Source
National Medical Device Policy, 2023
Simplifying the regulatory framework:
- The implementation of a "Single Window Clearance System" for licensing medical devices which would align with the National Single Window System (NSWS) to prevent redundant efforts and unnecessary compliance requirements
- The Bureau of Indian Standards (BIS) and sector-specific standards development organizations, will gradually expand the standards related to processes, products, wireless technologies, and performance. This expansion aims to improve standardization and quality, enabling the domestic industry to become globally competitive. The goal is to formulate and adopt Indian Standards for Medical Devices
- A framework will be developed to regulate pricing in a coordinated manner. This framework will align with the provisions of the Drugs (Prices Control) Order, 2013, through the National Pharmaceutical Pricing Authority (NPPA) to ensure that quality and effective medical devices are available to all citizens at affordable prices
- A guidance framework will be designed to assist researchers, innovators, and entrepreneurs in complying with regulations during the research and development phases of bringing market-ready products. This framework will be implemented from the design phase itself and will also cover testing purposes
- An institutional arrangement is envisioned to align the regulations of the National Medical Commission (NMC) and the industry associations' code of ethics
Building infrastructure:
- The establishment and enhancement of large medical device parks and medium-sized medical device clusters will be pursued. These facilities will be equipped with a state-of-the-art common infrastructure, located in proximity to economic zones with appropriate logistics connectivity. This initiative is in line with the National Industrial Corridor Program and the proposed National Logistics Policy 2021 under the PM Gati Shakti framework
- While some testing and certification facilities for medical devices are currently available in government institutions such as the National Institutes of Pharmaceutical Education and Research (NIPERs), Centres under the Department of Biotechnology, and Centres under the Indian Council of Medical Research, the aim is to facilitate the establishment and strengthening of an adequate number of testing laboratories specifically for medical devices. This initiative aims to ensure the quality, safety, and efficacy of medical devices marketed in the country
- Support will be provided for the phased manufacturing of critical components to ensure uninterrupted access and availability of medical devices, thus avoiding disruptions in the supply chain. The objective is to boost domestic manufacturing capabilities in the medical device sector
Developing skilled human resources:
- Capitalize on the resources available within the Ministry of Skill Development and Entrepreneurship's skill ecosystem to develop qualifications for skilling, reskilling, and upskilling professionals in the medical device sector. Certification of candidates/professionals based on these qualifications will be integrated into the National Skill Qualification Framework (NSQF), and all skilling courses will be aligned accordingly
- The policy will provide support for dedicated multidisciplinary courses focused on medical devices within existing institutions. This measure ensures the availability of skilled manpower for futuristic medical technologies, high-end manufacturing, and research. The goal is to produce MedTech human resources that are well-prepared for the sector's evolving needs
- In consultation with the industry, a National Database will be formulated and regularly updated to identify the various skills required for the latest manufacturing technologies used in the MedTech sector. This database will also encompass the skills necessary for the adoption of specific technologies
- A framework is envisioned to facilitate partnerships between academic institutions in the medical devices sector and foreign academic/industry organizations. These collaborations will focus on developing medical technologies, fostering innovation, and promoting knowledge exchange
Encouraging research and development:
- Encouraging structured interaction between academic institutions and the medical devices industry to create an environment conducive to industry-academia collaboration. This will foster the development of self-reliant technology products
- Coordinating the efforts of the government and industry to establish Centers of Excellence in premier academic and research institutions. These CoEs will contribute to the development of world-class institutions and attract global experts. The expertise available in these institutions will be leveraged to support product development and validate technology
- Exploring the establishment of innovation hubs that bring together a network of academic institutions, start-ups, clinical settings, funding agencies, and other stakeholders. These hubs will create a health technology ecosystem by providing plug-and-play infrastructure. Additionally, they will explore the use of 5G use-case labs
- Seeking convergence of available resources from various institutions such as the Biotechnology Industry Research Assistance Council (BIRAC), Start-up mission, AGNIi, and other enabling mechanisms. This convergence aims to promote innovation and commercialization in India, maximizing the utilization of government-funded inventions
Positioning the brands effectively and creating awareness:
- Undertake studies and projects to learn from successful global practices in manufacturing and skilling systems. The objective is to explore the feasibility of adopting such models in India, adapting them to suit the country's requirements
- Promote awareness regarding medical device safety and standards, while ensuring proactive communication and outreach to the public regarding the value proposition offered by medical devices
- Encourage the establishment of more forums that bring together various stakeholders to facilitate knowledge sharing and the development of robust networks across the sector. These forums will provide a platform for collaboration and collaboration among stakeholders, fostering innovation and growth
Attracting investments in the sector:
- Encourage private investments in the sector by establishing an ecosystem that supports risk-based or risk-adjusted financing. This will involve active outreach and engagement activities such as promoting seed capital and funding series from Venture Capitalists. VCs will also be invited to participate in the screening and incubation of start-ups
- Promote new financing models, including blended finance, which combines both public and private funds to support the sector
- Engage, leverage, and build upon various initiatives such as the Start-up mission of the Department for Promotion of Industry and Internal Trade to encourage the growth of start-ups in the medical devices sector
- Utilize initiatives like the Public Procurement (Make in India) Policy and the Ayushman Bharat program to leverage opportunities for domestic manufacturing and promote the production of medical devices within the country
- The Gazette of India - (https://pharmaceuticals.gov.in/sites/default/files/ Gazette%20Notification%20%20National%20Medical%20Devices%20Policy%202023.pdf)
- National Medical Device Policy, 2023 - (https://www.lexology.com/library/detail.aspx?g=75be96cd-af94-4526-9a02-919e53f6507f)
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