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 ...

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 announced risk classification of 187 medical devices pertaining to interventional radiology under Medical Devices Software, under the ...

In a major crackdown that has raised serious concerns over patient safety, officials in Telangana busted an unlicensed ...

During the raid, officers found the company manufacturing Risk Class-B medical devices without mandatory approvals ...

The medical device contract manufacturing industry is continuing to transform through 2024. A decade before COVID highlighted the critical nature of manufacturing infrastructure, there were investors ...

The Central Drugs Standard Control Organisation (CDSCO) has announced risk classification of 119 medical devices pertaining to radiotherapy under the Medical Devices Rules (MDR), 2017, as part of ...

Telangana: Drugs Control Administration, Telangana, has busted the unlicensed manufacturing of Medical Devices at Mediblue ...

The low labor cost of Chinese workers has been a key factor in the shift to manufacturing in China. Even after new minimum wage laws went into effect in parts of China in 2010, there is still a vast ...

The Telangana Drugs Control Administration raided an unlicensed medical device unit at Sultanpur in Sangareddy district and ...

Telangana DCA raids unlicensed medical device unit in Sangareddy, seizing ₹1.70 lakh worth of unauthorized products.

Regulatory overhaul aims to cut compliance burdens, improve safety, and attract investment in India’s $15B medical devices ...