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How to accelerate product development and regulatory approval process

June 11, 2015 @ 3:00 pm - 6:30 pm

| €130
bannière fda 682x268

How to accelerate your product development and its regulatory approval process?
The role of computer modeling and simulation

Do you actively develop medical devices, diagnostic solutions, tissue engineering products, medical equipment or pharmaceuticals?
Do you know that regulatory authorities recommend computer modelling and simulation to accelerate the regulatory approval process of new products?
Join us for this seminar to learn best practices adopted by innovative companies using engineering simulation to accelerate both product development and the regulatory approval process.

Today, more and more innovative products in respiratory, cardiovascular, orthopedic, diagnostic and neurologic sectors to mention a few benefit from computer modeling and simulation to speed product development and ease the regulatory approval process.
The Food and Drug Administration (FDA) and the European Medicine Agency (EMA) are aware of the challenges in bringing new treatments to market as quickly as possible without compromising patient safety. For many years, the FDA has recognized the potential value of computer-based clinical models and is encouraging the adoption of this technology.
BioWin, the health cluster of Wallonia, and the premium sponsor ANSYS, invites you to this afternoon session.
As a member of lifetech.brussels, partner of this event, beneficiate from a competitive price.

Agenda

15h00 – 15h30: Registration and welcome coffee

15h30 – 15h40: Presentation of the Health ecosystem in Wallonia and its main technological areas
Marianne Ghyoot – Associate Director, R&D and Process Management at BioWin
Laurence Timmermans – Innovation & Technological Partnerships Developer at BioWin

15h40 – 16h05: Growing importance of engineering simulation in the life sciences industry – Concrete examples
Thierry Marchal – Global Industry Director at ANSYS Inc
Case study 1: Implanted cardiovascular medical device
Boubker Ait Brik – Simulation department manager at Cardiatis
Case study 2: Bone regeneration and tissue engineering applications
Liesbet Geris – Professor at the Department of Aerospace and Mechanical Engineering at Université de Liège (ULg)

16h05 – 16h55: Use of simulation for the regulatory process approval – European Perspective
Adriano Henney – Executive Director at VPH Institute
Case study 3: Functional respiratory imaging
Jan Debacker – CEO at Fluidda

16h55 – 17h10: Coffee break

17h10 – 17h40: Use of simulation for the regulatory process approval – North America Perspective
Dawn Bardot – Senior Program Manager, Modeling & Simulation at Medical Device Innovation Consortium (MDIC)
Marc Horner – Lead healthcare specialist at ANSYS North America

17h40 – 18h00: Wrap-up & Panel Discussion

18h00 – 18h30: Cocktail & networking

 

Your objectives:

  • Gain awareness of computer modeling and simulation
  • Understand how regulatory authorities deal with this technology
  • Learn about the concrete benefits obtained by early adopters
  • Network with leaders using computer modeling and simulation
  • Challenge solution providers to assist you with your specific products.

Public targets:

  • Companies developing or with already existing products on the market
  • Regulatory affairs companies
  • Researchers working in mathematical modeling
  • Engineering services

Registration

Program and registration site

Details

Date:
June 11, 2015
Time:
3:00 pm - 6:30 pm
Cost:
€130
Event Categories:
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Event Tags:

Organizer

Biowin

Venue

Cercle du Lac – Léman Room
23 Boulevard Baudouin Ier, Louvain-La-Neuve, 1348
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