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Select article: Electronic Reporting of Adverse Event Data to the Food and Drug Administration: The Experiences of Glaxo Wellcome and Zeneca as Participants in the Adverse Event Reporting System Pilot Project

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First published October, 1999

Electronic Reporting of Adverse Event Data to the Food and Drug Administration: The Experiences of Glaxo Wellcome and Zeneca as Participants in the Adverse Event Reporting System Pilot Project

Mark Blake, Vlasta Pinkston

Therapeutic Innovation & Regulatory Science

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