Book Online Tickets for  Understanding FDA Design Verification a, Palo Alto. This webinar will help you understand specific product verification and validation requirements for medical devices to comply with ISO 13485: 2016 and FDA quality system regulations. It will focus on the topics such as product development process, tr

Understanding FDA Design Verification and Validation Requirements for Medical Devices

 

  • One Dial-in One Attendee

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    USD 179
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  • Group-Max 10 Attendees or Location

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    USD 449
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  • 1x Person - Unlimited viewing for 6 Months

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    USD 229
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  • One CD orUSB is for usage in one location only

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    USD 299
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  • Live + Recorded Version

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    USD 299
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  • Live + Training CD or USB

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    USD 349
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About The Event

This webinar will help you understand specific product verification and validation requirements for medical devices to comply with ISO 13485: 2016 and FDA quality system regulations. It will focus on the topics such as product development process, traceability and risk management at all stages, design outputs and documentation in DMR and DHR, design verification and design validation activity cycles and more.

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