The Food and Drug Administration (FDA) will offer a webinar entitled “Introduction to the Drug Master File (DMF)”.
On Monday, November 14, 2011, at 11:00am ET, the FDA Center for Drug Evaluation and Research (CDER) Small Business Assistance Program will present a 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.
Registration is required to view the webinar. To register, please visit the website: https://collaboration.fda.gov/dmf/event/registration.html
To participate in listen-only mode, please dial: