> ## 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-232/
- Published: 2019-08-04T12:00:00.000Z
- Updated: 2026-09-15T01:41:54.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5144692

[**Draft Guide on Clin-Pharm Considerations for Neonatals**](https://www.fdaweb.com/draft-guide-on-clin-pharm-considerations-for-neonatals/)  
*Federal Register* notice: FDA makes available a draft guidance entitled “General Clinical Pharmacology Considerations for Neonatal Studies for Drugs and Biological Products.” 08/02/2019

[**Nonclinical Toxicology Studies Q & A Draft Guide**](https://www.fdaweb.com/nonclinical-toxicology-studies-q-a-draft-guide/)  
*Federal Register* notice: FDA makes available a draft guidance entitled “Pathology Peer Review in Nonclinical Toxicology Studies: Questions and Answers.” 08/02/2019

[**Guide on Developing Bacterial Vaginosis Drugs**](https://www.fdaweb.com/guide-on-developing-bacterial-vaginosis-drugs/)  
*Federal Register* notice: FDA releases a final guidance on bacterial vaginosis drug development. 08/02/2019

[**Draft Guide on Drug Study General Considerations**](https://www.fdaweb.com/draft-guide-on-drug-study-general-considerations/)  
*Federal Register* notice: FDA makes available a draft guidance entitled “E8(R1) General Considerations for Clinical Studies.” 08/01/2019

[**Drug User Fee Rates Set by FDA**](https://www.fdaweb.com/drug-user-fee-rates-set-by-fda/)  
*Federal Register* notice: FDA establishes the prescription drug user fee rates for fiscal year 2020\. 08/01/2019

[**Info Collection Extension for Device GMPs**](https://www.fdaweb.com/info-collection-extension-for-device-gmps/)  
*Federal Register* notice: FDA seeks comments on an information collection extension for medical device GMP regulation. 07/31/2019

[**Info Collection Extension for UDI System**](https://www.fdaweb.com/info-collection-extension-for-udi-system/)  
*Federal Register* notice: FDA seeks comments on an information collection extension for “Unique Device Identification (UDI) System — 21 CFR Parts 16, 801, 803, 806, 810, 814, 820, 821, 822, and 830.” 07/31/2019