ANSYS - FDA - AVICENNA ROUNDTABLE
11/10/2019
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. |