sábado, 3 de septiembre de 2016

FDA Basics Webinar "FDA's MedWatch Program: Voluntarily Reporting Problems to the FDA"- Drug Information Update

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The Division of Drug Information (DDI)- serving the public by providing information on human drug products and drug product regulation by FDA.

Date: Sept 8, 2016 
Time: 1:00 pm EST
Did you know that you can report problems that you have had with drugs and other medical products to the FDA? Did you know that MedWatch can send safety alerts directly to you, as soon as they appear on the web site?
The featured speaker, Cristina Whalen Klafehn PharmD, BCPS, CDE, a Health Programs Coordinator in FDA’s Office of Health and Constituent Affairs will give an overview of the program, including recent updates, on the reporting of adverse events to the FDA.
For more information, please visit: FDA Basics Webinar.

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