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M-Corps Showcase Webinar: Integrated Computer Solutions (ICS)
Strategies to Limit Project Timeline and Cost in Medical Devices

Developing medical devices under a quality management system for the FDA can be a complicated and subtle process with tremendous variability. The leading mitigatable risk to budget and schedule comes from minimizing the impact of change during the development process. This presentation will address common categories of change and how to minimize or even benefit from the disruption.

About ICS:

ICS’s dedicated MedTech practice offers deep domain expertise, specialized tools, ISO 13485-compliant processes, and services to accelerate development, testing and certification.

Our experienced team of software developers, HFE specialists, UX and visual designers, and regulatory and cybersecurity experts create powerful MedTech solutions that help customers reduce costs and redundancies, enhance software performance, manage development complexity, stabilize new-product introductions, and navigate key regulatory standards, including ISO 62366 and IEC 62304. Companies like Quidel, Thermo Fisher, Boston Scientific and Millipore Sigma rely on ICS development support for their products.


Milton Yarberry, Director of Medical Programs, ICS

Milton is a certified PMP with a background in software architecture, medical device product development and program management. He spent a decade in consulting working with startup companies, and 15 years working with Class II and Class III medical device manufacturers. Milton’s work has been published in Medical Design and Outsourcing, Today’s Medical Developments and Design News.

Jan 19, 2022 01:00 PM in Eastern Time (US and Canada)

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