CDER SBIA invites you to join us for this two-day in-depth exploration into the world of pharmaceutical quality. Interact with FDA’s subject matter experts from our Office of Pharmaceutical Quality (OPQ) as we address topics such as:
Microbial Controls * Manufacturing Process * Facilities Assessment * Method Validation
* Register Here *
- Available for attendance in-person or virtually online -
Pre-approved by RAPS as eligible for up to 12 credits towards a participant’s RAC recertification uponfull completion
Hotel Block at discounted rate available until June 22nd
There is no cost to register. However, we ask that you honor your registration commitment.
Be sure to take advantage of this opportunity!
Registration is required for both in-person and online attendance.
The Small Business and Industry Assistance program in the Center for Drug Evaluation and Research (CDER SBIA) provides guidance and information to regulated domestic and international small pharmaceutical business and industry through its website, email notifications, and workshops. This notification system provides current information from CDER/FDA via e-mail on a biweekly basis that is relevant to small pharmaceutical business, which includes Federal Register notices, guidances, workshop announcements, etc. This is an automated message delivery system. Replying to this message will not reach the CDER SBIA staff. If you have comments or questions, please contact us Monday through Friday 8:00AM - 4:30PM.
Email: CDERSBIA@fda.hhs.gov
Phone: 1-866-405-5367
Phone: (301) 796-6707
Website: http://www.fda.gov/cdersbia
Phone: 1-866-405-5367
Phone: (301) 796-6707
Website: http://www.fda.gov/cdersbia
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