Medical Device Software Compliance Webinar

DUBLIN, 13 November 2023 /PRNewswire/ — The “3-Hour Virtual Seminar on IEC 62304 – Medical Device Software Compliance” webinar has been added to’s offer.



Explore the application of the IEC 62304 standard to medical device software and discover industry best practices for delivering reliable and secure medical device software solutions.

This session is designed for professionals in FDA-regulated industries including pharmaceuticals, medical devices, biologics, animal health, and tobacco.

Whether you work in research and development, manufacturing, quality control, distribution, clinical testing, governance, adverse event management or post-marketing surveillance, this webinar is tailored to your needs. It is important if you play a role in planning, executing, or managing the implementation of systems subject to FDA regulations, and equally beneficial to individuals responsible for maintaining or supporting such systems.

Stay on top of compliance requirements, increase your understanding of industry standards, and ensure the smooth operation of FDA-regulated systems by attending this highly informative session. Don’t miss this opportunity to expand your knowledge and expertise in this critical area.

Key topics covered:

  • Providing safe and effective medical devices is in the best interest of all those involved in the development of software for those products and of those involved in developing medical devices that use software

  • This session will provide insight into the IEC 62304 standard as it applies to medical device software

  • You will learn how to apply this standard to your own work processes

  • You will also gain insight into current industry best practices that will help you comply with IEC 62304

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Carolyn Troiano has more than 30 years of experience validating computer systems in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated industries. She is currently an independent consultant advising companies on computer systems validation and large IT system implementation projects.

For more information on this webinar visit

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