Simulation is more than Software

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in vivo, in vitro, in silico – Computational Modeling in medical device approval process

How simulation can save you time and money while increasing safety.

CADFEM Medical
Webinar
Structural mechanics
Structural mechanics
Overview of simulation, Scalability of simulations

In silico methods today are the key to faster and at the same time safer approval of medical devices. We show you how.

The CADFEM Medical webinar answers fundamental questions such as: "What is in silico, what can it achieve, what initiatives, regulations, standards and guidelines are already in place, and it provides insights into the regulatory situation in the EU and USA (application of ...

more details of product

Overview
Target group:
Users, Decision-makers, Students, Instructors, General enthusiasts
Prerequisites:
None
Applications:
Durability, Linear/Non-linear Simulation
Software used:
Ansys Mechanical
Target group
Users, Decision-makers, Students, Instructors, General enthusiasts
Prerequisites
None
Applications
Durability, Linear/Non-linear Simulation
Software used
Ansys Mechanical
Not the right offer? No suitable date? Whether webinar, live online info event, trial support or training - together we identify the best option for you.

Our offer in detail

  • What is "in silico"?
  • In silico methods, initiatives, standards & guidelines (FDA, MDIC, ASME, AA (GSP, structures to be established in the EU etc.)
  • In silico possibilities, state of the art examples

The CADFEM Medical webinar answers fundamental questions such as: "What is in silico, what can it achieve, what initiatives, regulations, standards and guidelines are already in place, and it provides insights into the regulatory situation in the EU and USA (application of simulation in the approval process).

In order to meet the constantly growing demands of the health care industry for medical products, more efficient methods in product development and evaluation are necessary. Computer-aided simulation studies have proven to be an adequate approach in addition to the established methods for testing. They already enable manufacturers to bring their products to market more quickly and at reasonable cost.

Examples are used to show what is possible and what is already being successfully practiced with the current state of the art.

The seminar is aimed at all engineers, project managers and Managers who want to use simulation methods in the development of medical devices in order.

  • Learning how simulation can be used in principle and which requirements are necessary for it
  • Learning new technologies and processes to support the approval of medical devices
  • Learn how to accelerate approval times without sacrificing safety
  • Optimizing the so-called Time to Market
Jan Hertwig
CADFEM Medical GmbH Grafing

Do you have questions concerning the webinar?

Germany

Administration

Austria

Seminar Administration

Switzerland / Liechtenstein

Additional offers

The right training, hardware and software add-ons are key to achieving a successful and swift introduction to simulation