Search for: "GIBBS v. GIBBS"
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22 May 2024, 7:07 pm
Gibbs & Ana Loloei & Véronique Li, Senior Medical Device Regulation Expert —We recently blogged about the Center for Devices and Radiological Health’s (CDRH) reluctance to make full use of real-world data (RWD) and real-world evidence (RWE) to support marketing applications. [read post]
22 May 2024, 2:09 pm
From Tilley v. [read post]
13 May 2024, 5:58 pm
Gibbs & Ana Loloei & Véronique Li, Senior Medical Device Regulation Expert —FDA has long touted the use of real-world evidence (RWE). [read post]
9 May 2024, 9:32 am
State v. [read post]
7 May 2024, 4:45 am
New trialR. v. [read post]
2 May 2024, 6:25 pm
Gibbs & Allyson B. [read post]
27 Mar 2024, 10:43 pm
Costs webinar from Kings Chambers’ Matthew Smith and Paul Hughes discussing how the judgment of the Court of Appeal in Kenig v Thomson Snell and Passmore LLP [2024] EWCA Civ 15 affects the way that solicitors ought to perform retainers dealing with the administration of estates and the likelihood and course of assessment of their […] The post Costs webinar on Kenig v Thomson Snell and Passmore LLP first appeared on Legal Costs Specialists - Gibbs Wyatt Stone. [read post]
25 Mar 2024, 11:00 pm
The Court of Appeal’s decision in Hadley v Przybylo [2024] EWCA Civ 250 is something of a curiosity. [read post]
22 Mar 2024, 4:00 am
Afflicted with a “culture of complacency[1],” the Ontario Superior Court has long struggled to timely advance cases to trial. [read post]
7 Mar 2024, 8:29 pm
By Véronique Li, Senior Medical Device Regulation Expert & Jeffrey N. [read post]
6 Mar 2024, 9:03 pm
[5] Commission Guidance Regarding Disclosure Related to Climate Change, Release No. 33-9106 (Feb. 2, 2010) [75 FR 6290 (Feb. 8, 2010)] [6] See Basic Inc. v. [read post]
11 Dec 2023, 8:33 pm
First, FDA notes that the Agency is “currently working to enhance our Third-Party Review Program, which was reauthorized under MDUFA V. [read post]
14 Nov 2023, 9:22 am
That’s the question the prosecutor asked a witness in State v Gibbs. [read post]
1 Nov 2023, 9:41 pm
Gibbs —For more than three decades, FDA has claimed that the Federal Food, Drug & Cosmetic (FD&C Act) gives the agency legal authority to regulate laboratory developed tests (LDTs) as medical devices (see our prior post here). [read post]
12 Oct 2023, 6:30 am
Frederick (2007) and Holder v. [read post]
23 Jul 2023, 7:55 am
Gibbs v. [read post]
7 Jul 2023, 11:28 am
Grove s v. [read post]
21 Jun 2023, 6:28 am
Gibbs, 402A21, ___ N.C. ___ (June 16, 2023). [read post]
19 Jun 2023, 7:19 pm
Gibbs & Allyson B. [read post]
