C. Records Second, Pfizer may be able to argue that it has better records than Rector. Courts have not consistently dealt with records as evidence of product identification. Courts are currently divided about whether plaintiffs must provide records to satisfy their product identification burden. Many courts have implied that a plaintiff must provide more than just their testimony to establish product identification. Mississippi Valley Silica Co. v. Reeves, 141 So. 3d 377, 383 (Miss. 2014); Osorio v. Baxter Int'l, Inc., 2011 U.S. Dist. LEXIS 48820, *2 (N.D. Ohio May 6, 2011). For example, in Reeves, the Court found that the plaintiff did not meet his burden on product identification because there were no records that the plaintiff ever interacted …show more content…
While plaintiffs may not have to provide any records at all, defendants appear to need to provide strong records to win at summary judgment. For example, in Wagoner, the plaintiff only presented evidence that his brother-in-law saw the product at the plant they worked out. Wagoner v. Exxon Mobil Corp., 813 F. Supp. 2d 771, 796-97 (E.D. La. 2011). The defendants put on testimony that the plant had never purchased that product before, but could not provide supporting records. Id. The Court found that this was conflicting testimony that the jury should hear and thus the Court denied summary judgment. Id. In contrast, if defendants can provide nearly conclusive documents, then they may win summary judgment. Nat'l Bank of Commerce of El Dorado, Arkansas v. Dow Chem. Co., 165 F.3d 602, 606-07 (8th Cir. 1999). For example, if a defendant could use records to show that the company had never bought the product then summary judgment likely would be appropriate for the defendant. …show more content…
One court found that New York’s mandatory generic drug law was conclusive proof that the plaintiff received a generic drug because the pharmacist had no choice, but to fill the prescription with generic drugs. Zandi v. Wyeth, No. A08-1455, 2009 WL 2151141, at *3 (Minn. Ct. App. July 21, 2009). In contrast, a different court found that West Virginia’s generic drug law was not conclusive evidence because it merely allowed a pharmacist to fill a prescription with a generic version of a drug. Keffer v. Wyeth, No. CIV.A. 2:04-0692, 2011 WL 1838966, at *3-4 (S.D.W. Va. May 13, 2011). Pfizer may be able to use Missouri’s generic drug statute as evidence against product identification. Unfortunately, Missouri’s statute is closer to West Virginia’s than it is New York’s because it is not mandatory. MO. ANN. STAT. § 338.056 (West 1996). Therefore, we likely cannot argue it is conclusive evidence that generic drugs were given to Rector. However, we can likely still use it as evidence as the statute does suggest a normal operating procedure of prescribing generic drugs. E.
In recent years, it has become an increasingly popular practice for drug companies to perform their clinical testing of new drugs in foreign countries that might not have the consumer protections or product liability laws present in the United States. Please answer each of the following questions using a theory studied in Module 2 specifically and thoroughly and using examples and facts from the readings and resources.
Forensic science evidence admissibility is when the forensic evidence can be used in the courtroom against a person. Any forensic science evidence that is admissible will be used in courtroom against that defendant. All types of evidence are shown to a judge or a jury to me a case against a suspect. Evidence that can be considered admissible, is any document, testimony, or tangible evidence used in a court of law. There are four types of evidence. The four types of evidence are demonstrative, documentary, real, and testimonial evidence. An example of demonstrative evidence is
Facts: In 1952 the United States was in a conflict in Korea, and the demand for steel
631F .3d 762 (2011), United States Court of Appeals, Fifth Circuit (January 21, 2011) .
Jan Hughes, Plaintiff-Appellant v, Boston Scientific corporation, Defendant-Apellee., 631F .3d 762 (2011), United States Court of Appeals, Fifth Circuit (January 21, 2011)
That the modification involved a subsequent remedial measure. involving the issue of whether the federal law requirement that generic drugs must bear the same FDAapproved labels as their brand-name counterparts preempts state law claims for failure to warn? Answer Selected Answer: That federal law preempted state law claims for failure to warn based on strict liability but that failure to warn claims based on negligence could proceed. That federal law preempted state law claims for failure to warn. Correct Answer:
The case involving Birch & Davis International, Inc., and Warren M. Christopher, the United States Secretary of State was decided on September 13th, 1993. The case involved procurement procedures conducted by the Agency of International Development (Open Jurist). The issue centered on exclusion of bids made by Birch & Davis International, Inc. Birch challenged the exclusion to the General Services Administration Board of Contract Appeals and they decided that the actions taken by the agency were fair. The case got to the Federal level when Birch appealed the decision by the board.
The California Board of Pharmacy report states:"RSF and SportPharm filled prescriptions for at least eighty-one (81) different physicians in 27 different states where the physician listed himself or herself as the patient in the prescription. These prescriptions were written by team physicians for professional and college sports teams throughout the United States and were apparently intended for office use and distribution by the physicians to either team staff or team players, despite the fact that each prescription indicates that the patient was the physician who wrote the prescription."
The carrier’s decision in denying coverage for the requested prescription Novolog 100 unit/ml cartridge was appropriate.
Often trails become controversial. When these court cases reach an end, people are either very satisfied or infuriated with the ruling or settlement that was determined. In the late 1990’s, a pharmaceutical company named Pfizer conducted trails on a new experimental drug in Kano, Nigeria. The drug was intended to be an alternative treatment to
The proposed Right-to-Try bill requires the federal government to allow for unrestricted access to investigational drugs, biological products, or devices to patients who are considered to have been diagnosed with a life-threatening illness when prescribed by a physician. The proposed law stipulates that the patient must have exhausted all other treatment options, and the investigational drug must have completed a
There was insufficient evidence to demonstrate that Barnes did understand the label to constitute a representation in the form suggested. It was found that Glendale was negligent and in all circumstances, it was considered there was a duty on Glendale to include in the packaging a warning as to the consequences of using corrosive product with hot water in a confined space such as a drain. There was no specific defect with the caustic soda but the issue is whether it was defective within the meaning of Section 75AC. It was found by the court the label to be defective within the meaning of section 75AC.
For a monthly subscription fee, the Aereo Inc. (the plaintiff) sells a service that allows subscribers to watch and record television programs around the same time that they are aired via the Internet. Aereo does not have a license from the copyright owners of the programs to record or broadcast their programs.
While this case is literally full of negative aspects, we will only focus on the main points for both arguments. Pharmaceutical companies want to be sure that the products they spend years and millions of dollars to create are not easily reproduced and sold at discount prices. The profits pharmaceuticals make of their patented products are supposed to refinance new research. So taking away their exclusive distribution rights and allowing other manufacturers to just copy the product and sell it at
Case Analysis: Blanchard Importing and Distributing Co. Inc. (HBS Case 9 - 673 - 033)