Develop a Quality Management System

A detailed QMS provides a structured framework that can help hospitals optimize the quality of patient care, reduce mistakes in the production process, and increase the credibility of point-of-care 3D printing labs. Register today and learn how to integrate a system of your own with training modules created by our Materialise experts, whenever and wherever you please.

Please note: These training modules are available for Materialise Medical software users only. Please contact us for all other inquiries.

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Who should attend

Professionals who use 3D printing at the point of care who

  • Want to build or enhance a process-based strategy for effective and efficient clinical service 
  • Want to positively impact patient care by adding quality assurance to their framework. 

Learning goals

  • Learn to build a quality management system that matches the additive manufacturing applications within your hospital’s existing framework. 
  • Discover how to integrate a QMS that focuses on existing and future legislation regulations, such as article 5.5 of the new Medical Device Regulation (MDR).* 
  • Benefit from Materialise’s 30+ years of experience as a device manufacturer meeting all necessary requirements while operating within a regulated QMS. 
  • Positively impact patient care by providing devices such as high-quality 3D-printed anatomical models. 

Training format

Course topics

An overview of quality management systems

Design quality assurance

Production quality assurance 

Technical documentation

MDR specific documentation**



*Training is intended to guide and instruct on existing regulations that may be relevant to point-of-care 3D printing. Acceptance or clearance of actual execution and audit of created processes and documentation is not guaranteed as part of this training. 

**One module contains specific MDR training and is designed for an EU audience

I software per dispositivi medici di Materialise potrebbero non essere disponibili in tutti i mercati, perché la disponibilità dei prodotti è soggetta alle prassi normative o mediche dei singoli mercati. Nei paesi in cui non è stata ottenuta la registrazione normativa di Mimics o 3-matic Medical, è disponibile una versione per la ricerca. Per domande sulla disponibilità di software per dispositivi medici Materialise nella tua area, contatta il tuo referente Materialise.L-101963-02