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Medical Device 2021 - IEC 62304 and Demystifying Software Validation using the Principles of LDLC - Medical Device classes online Training



VenueHollywood, Online Online



Topics/Call fo Papers

After waiting for seven or more months to find you’re device approval has been denied because the software section of the submittal is inadequate and not compliant is one of the biggest challenges device companies face today.
Medical device companies need to join this webinar to ensure that they know exactly what documentation needs to be prepared and submitted. They will also understand how to warrant that all documentation is prepared appropriately so the software portion of the submittal compliant to IEC 62304 regulations
Benefits of developing to an IEC62304 standard
What are the components of the Software Lifecycle
What are the major Software Work Products developed to the standard?
José Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences

Last modified: 2021-06-28 14:08:30