About FDA

DDI Webinar Series: “Collaborating with FDA- Get Involved with FDA’s MedWatch Adverse Event Reporting Program”- February 7, 2017

FDA’s Division of Drug Information in the Center for Drug Evaluation and Research (CDER) is excited to present a series of educational webinars targeting the needs of all healthcare professionals and students, including physicians, physician assistants, nurses, pharmacists, and pharmacy technicians. Interact with FDA staff from a variety of divisions and learn more about the FDA and drug regulation!

On February 7, 2017, CDER's Office of Communication, Division of Drug Information (DDI) hosted a webinar titled: Collaborating with FDA- Get Involved with FDA’s MedWatch Adverse Event Reporting Program. The featured speaker, Teresa Rubio, Pharm.D., is a Health Programs Coordinator in FDA’s Office of Health and Constituent Affairs. She gave an overview of the Office of Health and Constituent Affairs, Identified ways to advance FDA messages and be involved in FDA processes, and described how to report adverse events to FDA MedWatch, as well as obtain safety information.
Activity Outline and Continuing Education Information: Get Involved with FDA’s MedWatch Adverse Event Reporting Program (PDF - 40KB)

If you have never attended an Adobe Connect meeting before:

Test your connection: https://collaboration.fda.gov/common/help/en/support/meeting_test.htm

Get a quick overview: http://www.adobe.com/go/connectpro_overview 

Adobe, the Adobe logo, Acrobat and Adobe Connect are either registered trademarks or trademarks of Adobe Systems Incorporated in the United States and/or other countries.

Page Last Updated: 02/14/2017
Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English