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Biotech / Medical : Immunomedics (IMMU) - moderated -- Ignore unavailable to you. Want to Upgrade?


To: JJINV who wrote (49655)1/23/2019 2:10:51 PM
From: MFG ENG1 Recommendation

Recommended By
JJINV

  Respond to of 63283
 
"My comments: The FDA is kind of beating a dead horse here. We know IMMU was not great at preventing contamination"

I am not convinced anybody knows that. All conjecture at this point.. we have very little facts. The crucial word in my comment is "was". I KNOW IMMU was not great at preventing contamination as fact because the 483 told me so in clear words in at least 2 of their findings. You just have to be able to interpret the complaints the FDA had which I can because this is my life as a biomedical device manufacturing engineer. My hope is that Pehl and crew have turned this around and uncontrolled contamination will no longer be a specter in subsequent inspections by the FDA.

Would really like to see the actually CRL, and a complete response by IMMU magmt. Me too because then I would know the scope of what remediations they are still on the hook for and can better guess at a completion time for that. Is there any way to request this information through the Freedom of Information Act?

Sooner than later.



To: JJINV who wrote (49655)1/23/2019 3:06:18 PM
From: EMU21 Recommendation

Recommended By
JJINV

  Read Replies (1) | Respond to of 63283
 
Let me refer to kdd999's post # 49613. Which is from his research of FDA CRLs

The FDA never publicly discusses a CRL and companies never convey complete info about a CRL.

He goes on to explain why