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Experts Talk: Integrated MedTech Delivery from Requirements through Design to Quality Documentation
Unifying the numerous complex stages of product development is a vital challenge for innovators of medical technology. An integrated approach to MedTech product delivery is the key to navigating traceability, risk management, and quality control in a way that supports regulatory compliance and high product quality. Watch this Experts Talk webinar recording from 27 Nov…
Experts Talk: Balancing Innovation, Risks, and Compliance in Medical Device Development
Developers of medical devices and other medical technology are in a difficult spot. Not only are they operating at the cutting edge of technology innovation, an inherently risky business. But they must also meet regulatory compliance requirements of various local or international standards. To top it off, they have juggle those aspects while outpacing competitors…
How to improve Software Verification and Validation in Regulated Environments
In today’s world software development cycles are more and more shortened while the quality of products has to be increased and development costs have to be reduced to a minimum. These are seemingly unsolvable opposites. In the recording of this webinar held on 17 Sep 2019, speakers from Intland Software and Vector show how these…
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27 November 2019
Experts Talk: Integrated MedTech Delivery from Requirements through Design to Quality Documentation
13 November 2019
Experts Talk: Balancing Innovation, Risks, and Compliance in Medical Device Development
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