Mandatory Adverse Event Report via the SRP

Electronic Data Collection Using MedWatchPlus Portal and Rational Questionnaire--21 CFR 310.305, 314.80, 314.98, 514.80, 600.80, 1271.350 and Part 803

0645_Mandatory_pet_screenshot_3-11-2010[1]

Mandatory Adverse Event Report via the SRP

OMB: 0910-0645

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