DUBLIN, November 13, 2023 /PRNewswire/ — The webinar “3-hour virtual seminar on IEC 62304 – Medical Device Software Compliance” has been added to ResearchAndMarkets.com’s to 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 intended for professionals in FDA-regulated industries including pharmaceuticals, medical devices, biologicals, animal health, and tobacco.
Whether you work in research and development, manufacturing, quality control, distribution, clinical testing, management, adverse event management or post-marketing surveillance, this webinar is tailored to your needs. It is essential if you play a role in planning, executing or managing the implementation of systems subject to FDA regulations and is equally useful to individuals responsible for maintaining or supporting such systems.
Stay ahead of compliance requirements, increase your understanding of industry standards, and ensure seamless operation of FDA-regulated systems by participating in this highly informative session. Don’t miss this opportunity to expand your knowledge and expertise in this crucial area.
Main topics covered:
- Providing safe and effective medical devices is in the best interests of everyone involved in the development of software for these products, and of those involved in the development of medical devices that use software.
- This session provides insight into the IEC 62304 standard as it is applied 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
Speaker
Carolyn Troiano has more than 30 years of experience in the validation of 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 system validation and large-scale IT system implementation projects.
For more information about this webinar, visit https://www.researchandmarkets.com/r/p85ej3
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SOURCE Research and Markets
