Articles on Law, Science, and Engineering

Footnotes

1. "Products Liability for Medical Devices: Federal Preemption of State Lawsuits" 12 IEEE Engineering in Medicine and Biology, #2 p? (1993).[return to text]
2. Form 3500 and its instructions, The FDA Desk Guide for Adverse Event and Product Problem Reporting, can be obtained by calling 1-800-FDA-1088. Form 3500a and the interim instructions can be obtained from the Small Manufacturers section at the FDA, 1-301-442-6597.[return to text]
3. "Introducing MedWatch: A New Approach to Reporting Medication and Device Adverse Effects and Product Problems", JAMA, June 2 - Vol. 289, #21, p. 2765 (1993).[return to text]

    

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