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ANSYS - FDA - AVICENNA ROUNDTABLE

11/10/2019

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ANSYS - FDA - AVICENNA ROUNDTABLE

Roundtable discussion in Washington on 11 October 2019

For those of you who will be in Washington mid-October, ANSYS, in cooperation with the FDA and the Avicenna Alliance, is organizing a roundtable discussion titled "Transforming Computational Modeling from A Valuable Scientific Tool to A Valuable Regulatory Tool: Myth or Reality?".

The goal of the meeting is to discuss opportunities and challenges when utilizing in silico approaches during development and regulatory review.  The event will be organized around 2 panel discussions, where senior leaders from the largest medical device and pharmaceutical companies will be sharing their experience and expectations.

When and where: 11 October 2019, Marriott at Hyattsville Maryland (same hotel as BMES Conference).

Please register here to reserve your spot.

Do not hesitate to contact Krista Loeffler at krista.loeffler@ansys.com for more information.

AGENDA

Time Topic
9:30 AM REGISTRATION & BREAKFAST
10:00 AM - 12:00 PM How can Simulation play a more pervasive role in the Medical Device Industry?
Opportunities, challenges, and best practices for in silico approaches during development and regulatory review.
12:00 PM - 1:00 PM LUNCH
1:00 PM - 3:00 PM How can Simulation play a more pervasive role in the Medical Device Industry?
Opportunities, challenges, and best practices for in silico approaches during development and regulatory review.



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