Medical Device Industry in India: Past to Present

Bhat, Bhavana B; Prabhu, Pavithra Pradeep; Lobo, Manisha Joshel; Anusha,; Prathvi,; Kamath, B. Venkatesh

doi:10.5958/0974-360x.2019.01034.5

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Medical Device Industry In India States1

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2021

2022

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“…Total expenditure on healthcare in India stood at only 3.9% of GDP, compared with 8.9% in Brazil, 6.2% in Russia and 5.2% in China. Out-of-pocket expenses amount to 61%, with just 25% of the population insured [ 37 ]. While medical device firms focus mainly on increasing life expectancy and enhancing the quality of treatment, affordability for a wide range of impacts needs to be increased.…”

Section: Medical Device Industry In India Statesmentioning

confidence: 99%

Review on people’s trust on home use medical devices during Covid-19 pandemic in India

2022

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Section: Medical Device Industry In India Statesmentioning

confidence: 99%

Review on people’s trust on home use medical devices during Covid-19 pandemic in India

2022

View full text Add to dashboard Cite

Medical Device and Equipment Sector in India: Towards Sophisticated Digital Healthcare Systems—An Overview

Paul

2022

Next-Generation Nanobiosensor Devices for Point-of-Care Diagnostics

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Medical device’s regulation in South-East Asian countries: Current status and gap areas

Kalaiselvan

Aishwarya

Sharma

2021

AJPR

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As Medical device application in disease prevention, diagnosis or treatment is evolving to a greater extent; there is a need for regulation to monitor its quality, safety and efficacy. The present article attempts to study the medical device regulation available in eleven South-East Asian World Health Organization (WHO) member countries. The information searched from the available sources reveals that medical device regulation exists in seven countries. Most of the countries follow the International Organization for Standardization (ISO) 13485 for their quality standards in medical devices. Most countries also specified the time frame and authority to which adverse event is to be reported. Countries like India and Thailand have separate Adverse Event reporting forms for the medical device. The present study reveals that there is no separate web-based database for adverse event reporting of medical devices. Therefore, WHO South-East Asian Regulators Network (SEARN) under South East Regulatory Office (SERO) office may provide handholding support to these regions in developing a common software or tool for the management and analysis of signals arising from the adverse events.

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Medical Device Industry in India: Past to Present

Cited by 3 publications

References 0 publications

Review on people’s trust on home use medical devices during Covid-19 pandemic in India

Review on people’s trust on home use medical devices during Covid-19 pandemic in India

Medical Device and Equipment Sector in India: Towards Sophisticated Digital Healthcare Systems—An Overview

Medical device’s regulation in South-East Asian countries: Current status and gap areas

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