Tech-Talk: Best Practice - Medical Device Development & Integration of Regulatory Requirements
Online
Preis (zzgl. MwSt)*
free
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06 July 2023 4 - 5 pm (CET)

 Intended Purpose, User Needs & Requirements, Verification & Validation, Integration of Standards & Laws

 

Are you wondering how other companies document the development of medical devices in ALM software such as Polarion? In this webinar, we will show you a best practice approach that we have implemented in our new solution: avaMedical. It is based on our team's extensive experience from 8 years of Polarion implementation directly with medical device manufacturers, regulatory consulting projects and intensive exchange with Notified Bodies and manufacturers.

We will address all phases of product development and discuss documentation and its content, integration of content from other processes and regulatory information. Highlights in the webinar will include:

  • Which data and documentation model has proven itself for a digitized development process?
  • How will processes with interfaces to product development best integrate? How can processes with multiple interfaces be optimally integrated into product development?
  • How can a digital process increase regulatory compliance and support users in their daily work?

 

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Speaker | Organization
Sarah Panten
Sarah Panten
Strategic Business & Portfolio Development