GEM for Medical Device Industry

GEM for Medical Device Industry

The Government e-Marketplace (GEM) is a digital procurement platform launched by the Government of India to streamline the public buying process. For

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Refurbished Medical Devices

Refurbished Medical Devices: Law & Practices

Refurbished Medical Devices are becoming an important part of today’s healthcare system. Hospitals and clinics often need advanced equipment, but brand-new medical

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Clinical Data Required for Medical Device Approval

When Is Clinical Data Required for Medical Device Approval in India?

Clinical data required for medical device approval in India whenever a new, high-risk, or innovative medical device is introduced into the market.

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Oxygen Concentrator Manufacturing License

Oxygen Concentrator Manufacturing License

An Oxygen Concentrator Manufacturing License is a mandatory approval that manufacturers must obtain before producing and selling oxygen concentrators in India. These

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E-Commerce for Medical Device Industry

E-Commerce for Medical Device Industry

The E-Commerce for Medical Device Industry is growing rapidly as more companies and healthcare providers are moving towards online platforms. Earlier, medical

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Why EPR Certification Matters in Medical Devices?

Why EPR Certification Matters in Medical Devices?

EPR Certification matters in Medical Devices is one of the most important regulatory requirements today. EPR stands for Extended Producer Responsibility, which

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Make in India: Assembly or Manufacturing?

Make in India: Assembly or Manufacturing?

Make in India: Assembly or Manufacturing? The initiative was launched to build India as a global manufacturing hub. However, much of the

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Hazard Identification and Risk Assessment in Medical Device Design

Hazard Identification and Risk Assessment in Medical Device Design

Hazard Identification and Risk Assessment in Medical Device Design is a critical process that ensures medical devices are safe, effective, and compliant

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CDSCO Registration for Hearing Aids

CDSCO Registration for Hearing Aids

Hearing aids are classified as Class B medical devices in India and must be registered with the Central Drugs Standard Control Organization

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CDSCO Registration for Syringe Pumps

CDSCO Registration for Syringe Pumps

Syringe pumps are important medical devices used in hospitals to deliver medicines and fluids in very small and accurate amounts. Since they

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