Tandom
About
Sign inCreate a free account →
Tandom

The building blocks of global trade.

hello@tandom.ai

Proud to partner with

Microsoft for Startups

NVIDIA

Inception Program

Products

  • Tariff Calculator
  • AD/CVD Intelligence
  • HTS Classification
  • Document Intelligence
  • Entry Filing
  • Excel Plugin
  • Email Plugin

Catalogs

  • AD/CVD Catalog
  • HTS Catalog
  • Pending Investigations Directory
  • Rate Change Feed

Developers

  • API
  • AI Agent Workflows
  • MCP Connector
  • API Reference
  • API Pricing
  • API Changelog

Resources

  • Resource Center
  • Guides
  • Roadmap

Company & Legal

  • About
  • Privacy Policy
  • Terms of Service
  • Acceptable Use

© 2026 Fintora Technologies, Inc. d/b/a Tandom. All rights reserved.

Plain-English explanationMessage bodyFrequently asked questionsLearn more
  1. AD/CVD Catalog
  2. ›
  3. CSMS
  4. ›
  5. CSMS 51230259
CSMS 51230259·Operational·March 7, 2022·View on csms.cbp.gov ↗

FDA Launching New 24/7 Drug Entry Review Pilot

Plain-English explanation

CSMS 51230259 is a U.S. Customs and Border Protection (CBP) Cargo Systems Messaging Service bulletin (operational), published on March 7, 2022. It carries the official CBP guidance brokers and importers must follow for the topic — "FDA Launching New 24/7 Drug Entry Review Pilot". CSMS messages are the operational layer between Commerce determinations and at-the-border collections: when Commerce publishes a new rate, scope ruling, or instruction, CBP turns it into a CSMS that ACE/ACS systems and brokers act on.

Message body

Full text as published by U.S. Customs and Border Protection

CSMS #51230259 - FDA Launching New 24/7 Drug Entry Review Pilot U.S. Customs and Border Protection sent this bulletin at 03/07/2022 10:27 AM EST   Cargo Systems Messaging Service CSMS #51230259 - FDA Launching New 24/7 Drug Entry Review Pilot The volume of imported FDA regulated commodities continues to increase, driven in part by e-Commerce, trade volume and supply chain complexities which require ORA to assess our approach to import entry review.   The Food and Drug Administration’s Office of Regulatory Affairs’ Office of Enforcement and Import Operations (OEIO) is looking at several new ways to increase efficiency and effectiveness in our operational work. As part of this effort, OEIO has developed a 90-day pilot project to maximize our entry review staff at the periods of highest volume drug entries.     The Nationalized Drug Entry Review Pilot will run from March 13, 2022 through June 13, 2022. We will conduct entry admissibility reviews on a national basis versus the current port-by-port entry review approach. The pilot, which is being managed by OEIO’s Division of Food Defense Targeting, will utilize entry review staff over multiple time zones allowing us to expand our drug entry review coverage times to twenty-four-hour coverage per day, with 7 days per week staffing. We will cover all 336 ports of entry and this expanded coverage should allow for increased response time of drug entries. The pilot will also examine the potential to automate portions of the entry review process, allowing entry reviewers to focus more of their time on potentially higher violation products.   During the period of the Nationalized Drug Entry Review Pilot, FDA would also like to determine if efficiencies can be gained by receiving associated documentation at the time the entry is made rather than waiting for regular Documents Requested communications. We are calling this, The More We Know, The Faster You Go .   Our expectation is that the results and critical feedback from the pilot will provide OEIO with data to support potential changes to our entry review process.   We are excited about the prospects of this pilot and look forward to communicating more information on our results once the pilot has concluded. If you have any questions, please contact the new Nationalized Drug Entry Review Pilot at ERPilot@fda.hhs.gov or by phone (toll free) 833-312-3237 or 301-796-2249.   Update your subscriptions, modify your password or e-mail address, or stop subscriptions at any time on your Subscriber Preferences Page . You will need to use your e-mail address to log in. If you have questions or problems with the subscription service, please contact subscriberhelp.govdelivery.com . This service is provided to you at no charge by U.S. Customs and Border Protection . Privacy Policy | GovDelivery is providing this information on behalf of U.S. Department of Homeland Security, and may not use the information for any other purposes. Powered by Privacy Policy | Cookie Statement | Help

Frequently asked questions

What is CSMS 51230259?

CSMS 51230259 is a U.S. Customs and Border Protection (CBP) Cargo Systems Messaging Service bulletin titled "FDA Launching New 24/7 Drug Entry Review Pilot". CSMS bulletins are the operational instructions CBP issues to brokers, importers, and ACE filers covering rate changes, system updates, scope guidance, and other day-to-day customs-operations changes.

When was CSMS 51230259 published?

CBP published CSMS 51230259 on March 7, 2022. The bulletin's instructions are typically operative as of the publication date unless the body specifies a different effective date.

Is the CBP CSMS the legally binding instruction?

Yes — for at-the-border filing and entry collection. CSMS messages translate Commerce's Federal Register determinations into operational CBP instructions that ACE/ACS systems and brokers execute. The Federal Register notice is the underlying legal authority; the CSMS is the operational implementation. Both should be read together when reconciling a rate or scope change.

Learn more

Tandom guides relevant to CBP CSMS messages

Subscribe to and triage CBP CSMS messages

How to subscribe to CBP Cargo Systems Messaging Service and triage the messages that change broker filing behavior, without losing the ones that matter.

Open resource →

Real-time alerts when a CSMS message changes a duty rate

Set up alerts when a CBP CSMS message changes a duty rate on an HTS code you depend on. Built for brokers, forwarders, and importer compliance teams.

Open resource →

Find the right manufacturer or exporter rate in an AD/CVD order

Cash deposit cascade, separate rates, all-others, and PRC-wide rates. Worked example on case A-570-910 (galvanized welded steel pipe from China) with three exporter-specific rates.

Open resource →

Determine if a product is in scope of an AD/CVD order

Scope text is authoritative; the HTS list is illustrative. Read scope, find past rulings, and file a 19 CFR 351.225 inquiry. Worked example on case A-570-106 (wooden cabinets from China).

Open resource →

Bulk-classify SKU descriptions with the Tandom HTS Classifier API

Run thousands of product descriptions through HTS classification, score the confidence, and triage borderline rows. Public search endpoint plus the closed-beta three-layer Classifier.

Open resource →

Check AD/CVD exposure by HTS code

A practical workflow for checking antidumping and countervailing duty exposure on a US entry. For brokers and ops teams who need the answer before filing.

Open resource →