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IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF DELAWARE NOVARTIS PHARMACEUTICALS CORPORATION, et al., Plaintiffs,
V.
Salem, 465 F.3d 767, 777 (7 1h Cir. 2006); United States v. Brown, 415 F.3d 1257, 1269-70 (11th
Cir. 2005); Warner Chilcott Labs. v. Impax Labs., Inc., 2012 WL 1551709, *23-24 (D.N.J. Apr. 30, 2012). 1 Live testimony and cross-examination are much more likely to result in a correct decision from me about whether the expert is giving appropriate scientific testimony. Thus,
For the composition claims (that is, claims I, 2, and 7 of the '031 patent), if the limitation is that the ANDA product must contain "about 0.01 to about 0.5 percent by weight of an antioxidant" and the testimony is that the weight of the antioxidant in Par's product is 0.0016 percent, or less, it will be an interesting question whether there is literal infringement of those claims. See Cohesive Techs., Inc. v. Waters Corp., 543 F.3d 1351, 1368 (Fed. Cir. 2008).
while I am denying the motion for now, my understanding is that Defendant Par challenges the admissibility of the testing, and the conclusions drawn therefrom. Defendant may preserve this objection at trial by making an objection2 at the appropriate times during Dr. Davies' testimony. Failure to do so at the appropriate time will result in the objection being waived. The Court will consider granting a continuing objection. The Court will only consider evidence actually adduced at trial (whether through cross-examination or testimony from other witnesses) in ruling on any renewed motion. The Motion to Preclude (D.I. 251) is DENIED.