SkyQuest Technology Consulting published a report, titled, "Medical Device Contract Manufacturing Market - Global Opportunity Analysis and Industry Forecast, 2025-2032", valued at USD 78.9 Billion in ...

Overall, the classification of medical devices depends on two factors, i.e., the risk associated with device usage and the intended use of the device, along with any specialized indications for ...

The FDA will now be able to make the classifications based on the Asean Medical Device Directives, which classifies a device from A to D, depending on the risk it poses to the patients.

The Central Drugs Standard Control Organisation’s (CDSCO’s) draft rules for re-classification of medical devices based on their risk profile has received wide support from the industry, as it ...

With gowns, coveralls and adhesive drapes being classified in Class A category and surgical drapes being classified in Class B medical devices under Medical Device Rules (MDR-2017), regulatory experts ...

Dublin, Jan. 13, 2023 (GLOBE NEWSWIRE) -- The "The Global Market for Medical Devices, 12th Edition" report has been added to ResearchAndMarkets.com's offering. The Global Market for Medical ...

The Central Drugs Standard Control Organisation (CDSCO) has released an update on the existing risk based classification list of four categories, revisiting the existing list and adding new entries.

5. Medical Device Single Audit Program (MDSAP) Audits: These four- to five-day-long audits are meant to limit the number of countries that can audit a legal manufacturer.