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2 Nov 2009, 8:05 am
   In the US, the use of derivatives takes place every day and constitutes a fundamental business tool for both blue chip corporations and relatively small companies aiming at reducing their risk. [read post]
25 Apr 2015, 11:03 am by Schachtman
For example, in some litigations, plaintiffs will rely upon high-dose or high-exposure studies that are not comparable to the plaintiff’s actual exposure, and the defense may have shown that the only reliable evidence is that there is a small (relative risk less than two) or no risk at all from the plaintiff’s exposure. [read post]
11 Mar 2024, 6:30 am by Guest Blogger
”              There is no doubt that Hasen’s proposed amendment would cure, for once and for all, the lacunae announced (and embraced) by the Supreme Court in Bush v. [read post]
14 May 2015, 7:28 am
  If a treatment is so new that its risks and benefits cannot accurately be assessed, then a warning about its experimental nature is appropriate, but that kind of warning is a small subset of “off-label use” as an FDA regulatory status.Here is the article’s thesis:This Article proposes a fiduciary framework to regulate physician innovation under conditions of endogenous [we think that means “inherent” in this context] uncertainty. [read post]
11 Apr 2008, 9:00 am
No problem…: Lundbeck A/S v Generics UK Ltd & Ors: (IPKat), Exelon (Rivastigmine Tartrate) – Dr Reddy’s and Novartis settle Exelon patent dispute: (Therapeutics Daily), GeneMaker – Codon Devices, Blue Heron Biotechnology settle patent suit over gene synthesis platform: (Patent Docs), Glucophage (Metformin) – Depomed settles patent litigation against IVAX: (SmartBrief), (IP Law360), (GenericsWeb), Lexapro… [read post]
23 Mar 2012, 12:42 pm by Pace Law School Library
Critical habitat and the challenge of regulating small harms. 64 Fla. [read post]
2 Jul 2013, 1:41 pm
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