Dublin, Jan. 27, 2026 (GLOBE NEWSWIRE) -- The "An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Training Course (May 21, 2026)" training has been added to ...

This course is based on the 2016 version of the ISO 13485 Standard, providing skills necessary to perform internal process audits in the medical device industry. It features a detailed review of the ...

New self paced online courses cover medical device quality management, anti bribery management and management system auditing. ISO 13485 is the international standard for quality management systems in ...

The FDA has notified the medical device manufacturing sector that ISO-13485(2016) will be recognized as a Quality Management System Consensus Standard. In February 2026, the FDA will move away from ...

The medical device sector must meet stringent regulatory requirements plus convince potential customers that they make reliable, safe products. Having a strong commitment to quality can help customers ...

Globally, the medical industry is continuously growing and is highly dependent on technological advancements and essential procedures aimed at producing the best treatments. To make sure proper ...

eLeaP QMS gives medical device manufacturers the document control, design control, CAPA, and traceability tools needed to meet ISO 13485 requirements. LOUISVILLE, KY ...

Dublin, April 13, 2026 (GLOBE NEWSWIRE)-- The "An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices (May 21, 2026)" training has been added to ...