Search for: "In Re FD Processing"
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9 Dec 2018, 9:03 pm
Inspectors documented “a temperature inaccuracy during re-calibration of one Mercury In Glass thermometer that resulted in the potential under-processing of all LACF (low-acid canned foods) products manufactured by (the) firm between approximately Feb. 1, 2016 through Feb. 19, 2017. [read post]
12 Oct 2018, 10:26 am
In re Elysium Health-Chromadex Litig., 2018 WL 4907590, No. 17 Civ. 7394 (CM) (S.D.N.Y. [read post]
1 Feb 2018, 5:55 pm
This culminated in the decision in In re Trulia Shareholder Litigation, 129 A.3d 884 (Del. [read post]
8 Nov 2017, 3:04 am
” And if you’re into Reg FD, read my “Broc Tales Blog“… Reg FD in Japan: Coming Soon? [read post]
20 Sep 2016, 10:00 pm
When FDA re-inspected and re-sampled the SM Fish facility — Aug. 15 to Sept. 9 — testing results showed that Listeria was detected in 12 out of 116 locations, including on a direct food contact surface. [read post]
12 Jan 2016, 1:18 pm
Because grandparent visitation cases are often treated as “non-dissolution” or “FD” cases, a streamlined, form pleading process was created by the court to use in FD cases. [read post]
20 Nov 2015, 8:47 am
Kozlowski, 80 N.J. 378(1979); In re: Estate of Roccamonte, 174 N.J. 381 (2002); Devaney v. [read post]
13 Nov 2015, 4:54 am
Nope, we’re playing this one straight down the middle. [read post]
8 Sep 2015, 12:34 pm
But you’ve got to wait at least one week after the complaint is filed before you can get to the RD, and two weeks before you can get to the FD. [read post]
9 Apr 2015, 6:30 am
An operation is like a re-injury and it resets the biological clock. [read post]
13 Jun 2014, 5:00 am
Even widespread acceptance of an unapproved use in the medical community is no guarantee that the drug is safe or effective for that use, and is no substitute for the rigorous clinical trials, FDA-approved labeling, and careful scrutiny by FDA that the drug approval process requires.FDA Response at 5-6. [read post]
19 Dec 2013, 6:12 am
Notably, the “restricted device” definition not only includes devices with “requirements” imposed at the time of the PMA process, but also devices subject to FDA “performance standards. [read post]
25 Nov 2013, 7:04 pm
” What’s the “PGS” process? [read post]
16 Nov 2013, 9:30 pm
Amended ¶3-304.17(A) to clarify conditions under which the re-use of returnables are permitted. [read post]
14 Nov 2013, 7:41 am
Ct. 2567 (2011), so we’re not going over that again. [read post]
30 Jul 2013, 2:01 pm
July 29, 2013)andIn re Reglan Metoclopramide Litigation, 2013 Pa. [read post]
22 Jan 2013, 4:17 pm
In 2009, the CDRH began to re-evaluate its procedures for reviewing new medical devices. [read post]
26 Sep 2012, 6:44 pm
FDA did not previously have a process for suspending the registration of a food facility in such circumstances. [read post]
18 Jan 2012, 9:28 am
If you're in a multi-billion dollar market where every sale counts and maintaining market share is key, time is of the essence. [read post]
17 Jan 2012, 9:38 pm
On its website, Ameritox refers to its "Rx Guardian (SM) process. [read post]
