DUBLIN--(BUSINESS WIRE)--The "An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Training Course" conference has been added to ResearchAndMarkets.com's offering.

In recent years, general-purpose devices such as personal computers, smartphones and wearables have enabled the proliferation of “software as a medical device” (SaMD) products. The International ...

Experts Tell Device Companies Not to Fret Over QMS Transition Ahead of the proposed shift away from the current US Food and Drug Administration (FDA) quality management system (QMS) CFR 21 Part 820 ...

Medical device manufacturers are adopting integrated quality management systems that extend past compliance to drive cost ...

The Master of Engineering (M.Eng.) in Medical Device Development is a cutting-edge program that promises to accelerate the career development of aspiring engineers in all disciplines who wish to pivot ...

On Monday, February 2, a new final rule from FDA changing QMS requirements for medical devices went into effect. Manufacturers have had over two years to comply with the new rule, which is now full ...

Agile PLM supports continuous improvement, enhances visibility across the product lifecycle, and reduces the risk of costly errors. As a result, it is becoming a cornerstone of modern medical device ...

Anyone who has worked inside a MedTech organization knows that bringing a new device to market is not a single sprint. It is a marathon made up of dozens of short, fast, sometimes messy races — market ...

The main market opportunities include increasing demand for ISO 13485:2016 training, especially for new entrants or as a refresher for existing medical device professionals, offering a pathway for ...