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This article gives a brief on India’s Medical Device Grouping

This article referring to CDSCO/RRAS Ver.:00 dated 23/11/2012, talks about

This article gives a detailed overview on Disinfection and Antiseptic

Periodic Safety Update Reports (PSURs) submission process has significantly undergone

The Drugs & Cosmetics Act of 1940, underpinning the regulatory

Medical Device Sales in India are facilitated through the The

Learn More About CDSCO Medical Device Registration Process This article

National Single Window System (NSWS) – The Central Drugs Standard

The National Pharmaceutical Pricing Authority (NPPA) in India is a regulatory body responsible

Introduction: Policy 2023 intends to support the Medical Device industry’s

This article is about MDR India for a notice published

Introduction The process of medical device registration in India is

Introduction This Article deals with Class A Non-Sterile/Measuring Medical Devices

Introduction – Import of Medical Devices into India This article deals

Introduction – Voluntary / Non-Notified Registration of Medical Devices in