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FAQs by CDSCO: Key Highlights and Updates
Learn More About CDSCO Medical Device Registration Process This article
National Single Window System (NSWS), India
National Single Window System (NSWS) – The Central Drugs Standard
Price Capping in India by NPPA
The National Pharmaceutical Pricing Authority (NPPA) in India is a regulatory body responsible
Cabinet approves the Policy for the Medical Device Sector
Introduction: Policy 2023 intends to support the Medical Device industry’s
Amendment in the Drug Rules, CDSCO, MDR India
This article is about MDR India for a notice published
FAQ about Medical Device Registration in India
Introduction The process of medical device registration in India is
Exemption of Class A Non-Sterile/Non-Measuring Medical Devices from Licensing Regime
Introduction This Article deals with Class A Non-Sterile/Measuring Medical Devices
Import of Medical Devices into India
Introduction – Import of Medical Devices into India This article deals
Voluntary Registration of Medical Devices in India
Introduction – Voluntary / Non-Notified Registration of Medical Devices in
India Risk Classification for Operation Theatre as a Medical Device
Introduction – Operation Theatre Equipment Classification in India The importance
Unique Device Identification Number
What is a Unique Device Identification Number ? This blog
Mandatory Registration India – Amendment
Introduction: Non-Notified Registration India – Amendment This article deals with
India Risk Classification for Dermatology and Plastic Surgery as a Medical Device
Introduction – Dermatology and Plastic Surgery Equipment Classification in India
India Risk Classification for Rheumatology as a Medical Device
Introduction – Rheumatology Equipment Classification in India This article discusses
India Risk Classification for Interventional Radiology Products
Introduction – Interventional Radiology Equipment Classification in India The classification