> ## Content Index
> Fetch the complete content index at: https://www.foodconsumer.org/llms.txt
> Use this file to discover other available public pages before exploring further.

# CDER SBIA Webinar on “Overview of FDA’s Proprietary Name Review Process”
- URL: https://www.foodconsumer.org/fda_s_proprietary_name_review_process_0701141155/
- Published: 2014-07-01T12:55:00.000Z
- Updated: 2026-09-15T14:16:38.000Z
- Description: A notice for a CDER Small Business and Industry Assistance webinar on FDA's proprietary name review process, covering draft guidance meant to help sponsors develop drug brand names that are not misleading and do not contribute to medication errors.
- Author: Food Consumer
- Tags: Miscellaneous, Health News, #vivvo-import

On **Monday July 7, 2014** at 1:30 pm EDT, CDER SBIA will host a webinar entitled***“***Overview of FDA’s Proprietary Name Review Process.”

FDA published a notice in the *Federal Register* announcing the availability of the draft[*Guidance for Industry - Best Practices in Developing Proprietary Names for Drugs.*](http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM398997.pdf?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery)

This webinar will provide an overview of the Proprietary Name Review guidance that focuses on the safety aspects in the development and selection of proposed proprietary names for all prescription and nonprescription drug products and biological products. The draft guidance provides a qualitative systematic framework for evaluating proprietary names before submitting them for FDA review. FDA is issuing this guidance to help sponsors of drug and biological products develop proprietary names that are not potentially misleading and do not cause or contribute to medication errors. This webinar will go over the guidance that represents FDA’s current thinking on this topic.

**To register for this Event**, please go the following link: [https://collaboration.fda.gov/sbia070714/event/registration.html](https://collaboration.fda.gov/sbia070714/event/registration.html?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery)

(Registration password needs to be 8 characters and alphanumeric)

**Note: Your registration acknowledgement will include the webinar access link.** 

Audio will broadcast from your computer speakers.

Closed captioning will be provided.

Please note: There is a user capacity limit for this webinar. For those who cannot enter the webinar, please know that it will be recorded and a link will be posted to this page.

**Questions/Comments can be submitted live via a Q/A chat window**.

\- FR Document: [2014–12348](http://www.gpo.gov/fdsys/pkg/FR-2014-05-29/pdf/2014-12348.pdf?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery)

\- Docket ID: [FDA-2014-D-0622](http://www.regulations.gov/?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery#%21documentDetail;D=FDA-2014-D-0622-0001)

\- [Draft Guidance for Industry: Best Practices in Developing Proprietary Names for Drugs](http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM398997.pdf?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery)

For questions concerning the webinar, please contact CDER SBIA at:

[(866)-405-5367](tel:%28866%29-405-5367) | [(301)-796-6707](tel:%28301%29-796-6707)

CDER SBIA webinar series: [http://www.fda.gov/Drugs/DevelopmentApprovalProcess/SmallBusinessAssistance/ucm070334.htm](http://www.fda.gov/Drugs/DevelopmentApprovalProcess/SmallBusinessAssistance/ucm070334.htm?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery)