This seminar helps to bring medical device software that uses artificial intelligence (AI) methods to market quickly and in compliance with the law, although the regulatory requirements are still unspecific.

Goals

The seminar provides participants with the necessary knowledge to meet the regulatory requirements of software that uses machine learning (ML) methods. The seminar enables the participants to

  • to avoid regulatory problems during audits ,
  • to communicate with auditors and examiners on an equal footing ,
  • Minimize problems with the approval of the products and
  • Reducing effort and costs in data collection and development.

As a participant, you benefit from the seminar in which you

  • know the regulatory requirements for ML software,
  • be able to formulate the purpose of your software in accordance with the law,
  • be able to derive suitable quality metrics from this,
  • know how to describe and evaluate (training) data,
  • be able to select suitable machine learning methods,
  • know how to train and validate models in compliance with the law,
  • know and be able to evaluate suitable test procedures for the validation of ML libraries
  • understand how to ensure the "transparency" and "explainability" of your models and
  • who can monitor the products in the market (post-market surveillance).

Here you will find further information on the next dates, costs and registration. If nothing else is noted in the table on the overview page, there are still places available.

KONTAKT:
Online Seminar

 

Mehr Informationen