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Wednesday, November 9, 2011

Drug Information Update - CDER Small Business Update: Introduction to the Drug Master File Webinar, November 14, 2011


-----Original Message-----
From: U.S. Food & Drug Administration (FDA)
Sent: 11/9/2011 9:22:29 PM
To: guyperea@live.com
Subject: Drug Information Update - CDER Small Business Update: Introduction to the Drug Master File Webinar, November 14, 2011
Drug Information Update - CDER Small Business Update: Introduction to the Drug Master File Webinar, November 14, 2011

FDA Division of Drug Information: Know the Moment It Happens

The Division of Drug Information (DDI) is CDER's focal point for public inquiries. We serve the public by providing information on human drug products and drug product regulation by FDA.


Introduction to the Drug Master File (DMF) Webinar - November 14, 2011 

 

On Monday, November 14, 2011 at 11:00 a.m. (ET), our CDER Small Business Assistance Program will present our webinar entitled Introduction to the Drug Master File (DMF) which will discuss all aspects of filing a DMF, including when and why to submit a DMF; requirements and recommendations for formatting and submitting original DMFs and subsequent submissions; how DMFs are reviewed and common problems.

 

Our presenter will be Dr. Arthur Shaw who is CDER’s DMF Expert, in addition to being a Quality Reviewer in the Office of New Drug Quality Assessment (ONDQA).  He has extensive experience in dealing with DMF filing and database issues, as well as reviewing many DMFs for technical content as part of his daily review work to support New Drug Applications (NDAs) and Investigational New Drug (IND) applications.

 

Dr. Shaw’s previous positions in FDA include Special Assistant in the Office of New Drug Chemistry and Review Chemist in the Division of Gastrointestinal and Coagulation Drug Products and in the Division of Pulmonary and Allergy Drug Products. Dr. Shaw received a B.S. in chemistry (with Honors) from the City College of New York and a Ph.D. in biochemistry at Cornell University.

  

Registration website: https://collaboration.fda.gov/dmf/event/registration.html

 

Web Address for viewing on day of event: https://collaboration.fda.gov/dmf/event/login.html


Call in numbers (listen only mode):
 

Domestic: 1-800-857-0171

International: 1-517-319-9290     

Password (verbal): 2718839

 

For More Information: 

http://www.fda.gov/smallbusinessdrugs

Click on Workshops and Webinars in Spotlight box

 


This is an automated message delivery system.  Replying to this message will not reach DDI staff.  If you have comments or questions, please contact us at: 1-888-INFO FDA (1-888-463-6332) or (301) 796-3400 from 8:00 am - 4:30 pm Monday - Friday.  You can also email us at druginfo@fda.hhs.gov.


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