The U.S. Food and Drug Administration (FDA) categorizes medical devices into three classes based on the level of risk the devices pose to patients and users. Image Credit: IGORdeyka/Shutterstock.com ...
The Central Drugs Standard Control Organisation (CDSCO) has announced risk classification of 187 medical devices pertaining to interventional radiology under Medical Devices Software, under the ...
In recent years, there has been a growing emphasis on sustainability across the healthcare industry, and the medical device manufacturing sector is no exception. As the world faces environmental ...
The Central Drugs Standard Control Organisation (CDSCO) has launched a new risk classification module on the drug regulator's online system for medical devices in order to simplify the regulatory ...
Telangana: Drugs Control Administration, Telangana, has busted the unlicensed manufacturing of Medical Devices at Mediblue ...
The Telangana Drugs Control Administration raided an unlicensed medical device unit at Sultanpur in Sangareddy district and ...
Regulatory overhaul aims to cut compliance burdens, improve safety, and attract investment in India’s $15B medical devices ...
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