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Products Liability: Pharmaceutical and Medical Device Issues--2005

Substantive issues addressed by these materials include causation and non-personal-injury and other damages. Among the substantive topics of discussion are several that are specific to drug and medical device cases: liability when a manufacturer advertises prescription drugs directly to consumers; the effect of drug development processes and pre- and post-release testing on how liability is imposed; and scope of a manufacturer’s duty to warn. CL038

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Coursebook Papers:

Direct-to-Consumer Advertising Liability Revisited (20 pp) $29.00

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Electronic Discovery in Drug Cases (14 pp) $29.00

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Selected Cases (61 pp)

From Daubert to Verdict: Eight Steps to Success in Drug and Device Cases (12 pp) $29.00

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Causation in Pharmaceutical Cases (125 pp) $49.00

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Clinical Trials - Why They're Done, What They Tell Us, and What They Don't Tell Us (11 pp) $29.00

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Special Evidentiary Considerations for the Use of Lay Experts and Opinions: A Trap for the Unwary (26 pp) $29.00

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Limitations on the Duty to Warn: New Developments and Idiosyncratic and Allergic Reactions (25 pp) $29.00

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The Recent Expansion of Traditional Products Liability-Personal Injury Claims into More Complex Claims and Investigations (15 pp) $29.00

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The Fracture That Will Not Heal: The Landscape of Federal Preemption In the Fields of Medical Devices, Prescription and Over-the-Counter Drugs Ten Years After Medtronic, Inc. v. Lohr (24 pp) $29.00

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The Class Action Fairness Act of 2005 (“CAFA”) (7 pp) $29.00

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