Drugs

CDER Small Business and Industry Assistance (CDER SBIA) Webinar - Revised Draft Guidance for Industry: Submission of Quality Metrics Data

Image of SBIA Webinar 2016

 

The Food and Drug Administration, Center for Drug Evaluation and Research and Small Business and Industry Assistance (CDER SBIA), invites you to our webinar series.

These events focus on a specific topic and provide an opportunity for small business and industry entities to learn more about the FDA and basic drug regulation. The webinars support CDER SBIA’s mission of promoting productive interaction with regulated industry by assisting small pharmaceutical business and industry with information relating to the development and regulation of human drug products.

CDER is making available the webinar "Revised Draft Guidance for Industry: Submission of Quality Metrics Data" which provides an overview of and summarizes changes in the revised draft guidance.

Speakers:

Michael Kopcha, Ph.D., R.Ph.
Director
Office of Pharmaceutical Quality (OPQ)
Center for Drug Evaluation and Research (CDER)
Food and Drug Administration (FDA)

Tara Gooen Bizjak
Senior Science Policy Advisor

Division of Regulations, Guidance, and Standards

Office of Policy for Pharmaceutical Quality (OPPQ) | OPQ | CDER | FDA

Alex Viehmann
Acting Branch Chief
Division of Quality Intelligence and Risk Analysis and Modeling,
Office of Surveillance (OS) | OPQ | CDER | FDA

For questions concerning the webinar, please contact CDER SBIA at:
(866)-405-5367 | (301)-796-6707

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Page Last Updated: 12/13/2016
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