This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

Regulation, Clinical and Software for Medical Devices
November 5 - 7, 2024
Digital Conference8:00AM CST // 9:00AM EST // 2:00PM GMT

Matt Trachtenberg
Senior Director of Regulatory Affairs at Tempus AI
Speaker

Profile

Matt Trachtenberg is the Senior Director of Regulatory Affairs at Tempus AI where he serves as the regulatory leader for the Artificial Intelligence Business Unit (BU). There he leads regulatory strategy and execution to bring to market novel Software as a Medical Device in both radiology and cardiology. Prior to joining Tempus, he worked at Becton, Dickinson and Company (BD) in the Specimen Management (blood collection tubes/needles) and Diabetes Care (insulin patch pumps, mobile medical apps, clinical decision support) BUs. He is a former FDA device reviewer from the Division of Cardiovascular Devices and earned his Bachelor’s and Master’s degrees in Biomedical Engineering from the Johns Hopkins University.

Matt Trachtenberg's Network

Agenda Sessions

  • The Latest News: Regulating Medical Device Software (MDSW) in the US

    8:40am