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

# Latest Federal Register Notices
- URL: https://www.fdaweb.com/latest-federal-register-notices-195/
- Published: 2018-09-16T12:00:00.000Z
- Updated: 2026-09-15T00:32:10.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5142372

[**Guide on Consensus Standards Recognition/Withdrawal**](https://www.fdaweb.com/guide-on-consensus-standards-recognition-withdrawal/)  
*Federal Register* notice: FDA makes available a draft guidance entitled “Recognition and Withdrawal of Voluntary Consensus Standards.” 09/14/2018

[**Draft Guide on 510(k) Third-Party Review Program**](https://www.fdaweb.com/draft-guide-on-510-k-third-party-review-program/)  
*Federal Register* notice: FDA makes available a draft guidance entitled “510(k) Third-Party Review Program.” 09/14/2018

[**FDA Posts ANDA Bioequivalence Study Guides**](https://www.fdaweb.com/fda-posts-anda-bioequivalence-study-guides/)  
*Federal Register* notice: FDA makes available additional draft and revised draft product-specific guidances that recommend bioequivalence study designs that are intended to support ANDAs. 09/14/2018

[**Guide on Voluntary Consensus Standards**](https://www.fdaweb.com/guide-on-voluntary-consensus-standards/)  
*Federal Register* notice: FDA makes available a final guidance entitled “Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices.” 09/14/2018

[**FDA Proposed Rule to Improve FOIA Process**](https://www.fdaweb.com/fda-proposed-rule-to-improve-foia-process/)  
*Federal Register* proposed rule: FDA proposes to amend current regulations to incorporate changes made to the Freedom of Information Act by recent laws. 09/13/2018

[**Science Board to Hear CVM Antibiotic Resistance Response**](https://www.fdaweb.com/science-board-to-hear-cvm-antibiotic-resistance-response/)  
*Federal Register* notice: FDA announces a 10/22 public advisory committee meeting of its Science Board. that will hear a response from CVM on recommendations about antibiotic resistance monitoring. 09/13/2018

[**Proposed Rule on Device Electronic Submissions**](https://www.fdaweb.com/proposed-rule-on-device-electronic-submissions/)  
*Federal Register* proposed rule: FDA proposes to amend requirements for medical device premarket submissions to remove paper and multiple copies and replace them with requirements for a single submission in electronic format. 09/13/2018