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MikeCr

09/15/18 12:05 PM

#98401 RE: Sloan89RH #98395

Sloan, thanks for asking that question. I'd like to know also about OvaDx. I was hoping that was the test that Mark met with the FDA about in July. But TravO wrote that Mark said that the FDA submission was not for an individual test, more like product line.

Although in the tweets they referred both to "our test" and a "product line"
It's confusing

@arrayit Jul 2
Arrayit CLIA clinical team meets with top brass at the United States Food and Drug Administration FDA to discuss FDA approval of a major product line.

@arrayit Jul 3
Arrayit provides 7/2/18 FDA update: (1) excellent meeting, (2) large attendance by FDA top brass, (3) insightful and instructive, (4) our entire clinical team wishes to thank the agency for their feedback and generosity, and (5) we believe that our test will receive FDA approval.
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TravO

09/15/18 3:18 PM

#98411 RE: Sloan89RH #98395

Not so much on approval process for OvaDx.

But when I brought up Avant, he said as far as Avant goes, they hope Avant does well considering they have ownership in the company.

If Avant does well obviously it is beneficial for them as well.

I brought up OvaDx and other forms of cancer testing