The Impact of the Latest FDA Regulations on Laboratory Developed Tests (LDTs) for Patient Management

When:  Jun 10, 2024 from 12:00 to 13:00 (ET)

Please join us for an Open Scientific Discussion (OSD) hosted by the AAPS Gene and Cell Therapy Products (GCTPs) and Biomarkers and Precision Medicine (BPM) Communities on the following topic:

The Impact of the Latest FDA Regulations on Laboratory Developed Tests (LDTs) for Patient Management

What are LDTs and their roles in clinical trials?

What are the recent changes in FDA regulations?

How would this impact us?

Discussion Leaders:

Kelly Gordon (Boudicca Dx)

Mark Ma (Rallybio)

Mark E. Arnold (Bioanalytical Solutions Integration)

Organized by:  

Yan Ni (Passage Bio)

Yanmei Lu (Sangamore)

Carmen Fernandez-Metzler (PharmaCadence Analytical Services)

 

We start at 12:00 EST sharp. To avoid interruptions, please dial in before noon and mute yourself until Q&A starts.

(Please remain on mute unless asking questions)

When: Monday June 10, 2024, 12 pm – 1 pm EST

WherePlease join from your computer, tablet or smartphone.

https://meet.goto.com/505947717

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+1 (646) 749-3122
Access Code: 505-947-717

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Meeting ID: 505-947-717
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Please feel free to share with colleagues who may be interested in this topic. Thank you!

The AAPS GCTPs and BPM Community Leadership Teams

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