FDAs MedWatch Program: Voluntarily Reporting Problems to the FDA

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MedWatch Health Office of Regulatory Affairs Center for Drug Evaluation and Research Center for Veterinary Medicine Adverse Event Reporting System Adverse effect Food and Drug Administration Pharmaceutical sciences Clinical research		FDAs MedWatch Program: Voluntarily Reporting Problems to the FDA Add to Reading List Source URL: www.fda.gov. Download Document from Source Website File Size: 2,49 MB Share Document on Facebook