> ## 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.

# 18 FDA Info Collections Ok’d by OMB
- URL: https://www.fdaweb.com/18-fda-info-collections-okd-by-omb/
- Published: 2023-10-10T12:00:00.000Z
- Updated: 2026-09-14T19:01:27.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5155532

*Federal Register* notice: FDA is publishing a list of 18 information collections that have been approved by the Office of Management and Budget under the Paperwork Reduction Act of 1995\. They are:

- Premarket Notification Submission 510(k), Subpart E
- Good Manufacturing Practice Regulations for Type A Medicated Articles
- Tradeoff Analysis of Prescription Drug Product Claims in Direct-to-Consumer and Healthcare Provider Promotion
- Endorser Status and Actual Use in Direct-to-Consumer Television Ads
- Assessing Physiological, Neural and Self-Reported Response to Tobacco Education Messages
- Imports and Electronic Import Entries
- Current Good Manufacturing Practices for Blood and Related Regulations for and Blood Components; and Requirements for Donor Testing, Donor Notification, and Lookback
- Administrative Practices and Procedures; Formal Hearings
- Adverse Experience/Events with Approved New Animal Drugs
- Adverse Event Program for Medical Devices (Medical Product Safety Network (MedSun))
- Human Cells, Tissues, and Cellular and Tissue-Based Products
- New Animal Drugs for Minor Use and Minor Species
- Potential Tobacco Product Violations Reporting Form
- Food and Drug Administration Advisory Committee Regulations
- Accreditation Scheme for Conformity Assessment Program
- Quantitative Research on Front of Package Labeling on Packaged Foods
- Current Good Manufacturing Practice Regulations for Medicated Feed
- Medical Devices--Voluntary Improvement Program

To view the notice, click [here](https://public-inspection.federalregister.gov/2023-22465.pdf?ref=fdaweb.com).