- Medical Device Registration 2026

Custom Clearance Issues for Medical Devices

Custom clearance issues for medical devices are one of the most common challenges faced by importers in India. Since medical devices directly

European Authorized Representative for Medical Device Companies

A European Authorized Representative for Medical Device Companies is essential for non-EU manufacturers who want to sell their products in Europe. Under

Medical Device Regulations, 2017: Latest Law with Amendments

The Medical Device Regulations, 2017 (MDR 2017) were introduced by the Ministry of Health and Family Welfare to create a structured legal

MedTech Mitra Incubation

MedTech Mitra Incubation is a government-backed initiative launched in India to support innovators, startups, and researchers in developing affordable and high-quality medical

Medical Device Parks in India

Medical Device Parks in India are special industrial hubs developed by the government to boost local manufacturing of medical devices. These parks

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

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

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.

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

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