Why Choose Liberty Management Group Ltd.?

Why Choose Liberty Management Group Ltd. (LMG)?

Liberty Management Group Ltd. (LMG) is a globally recognized FDA, CE Marking, and ISO consulting firm headquartered in Aurora, Illinois, USA, with associates and offices around the world. Since 2009, LMG has successfully completed over 15,000 projects — helping domestic and foreign establishments navigate FDA regulations accurately, efficiently, and at a transparent, fixed price.

A Full-Service FDA Consulting Partner

Whether you need FDA registration, US FDA Agent representation, label review, drug listing, NDC labeler code requests, renewal management, or regulatory strategy, LMG handles it all under one roof. Our experienced consultants cover every FDA-regulated product category — food, drugs, medical devices, biologics, and cosmetics — so you never have to coordinate between multiple firms.

We serve manufacturers, importers, exporters, private label distributors, and brand owners in more than 150 countries, from first-time registrants to established companies managing ongoing compliance obligations.

Transparent, Fixed-Price Fees — No Hourly Surprises

One of the most common frustrations with regulatory consulting is uncertainty around cost. LMG eliminates that entirely. We provide an accurate, fixed-price estimate for every project before work begins — no hourly consulting fees, no hidden charges, no uncertainty.

All of LMG’s service fees are published openly on the LMG website, so you can calculate the total cost of your project before you even contact us. What we quote is what you pay.

Experienced Consultants, Accurate Guidance

Our consultants bring deep, hands-on experience across FDA regulatory programs. We stay current with regulatory changes — including the QMSR transition under 21 CFR Part 820, MoCRA requirements for cosmetics, GDUFA III fee changes, and ongoing FDA guidance updates — so the advice you receive reflects the current regulatory environment, not last year’s rules.

Free FDA Registration Certificate

After completing every FDA registration on your behalf, LMG issues a free registration certificate (PDF) for your records. This is a private confirmation of the work completed — not an FDA endorsement, but a useful internal record of your registration.

Free FDA Compliance Tools

LMG provides a suite of free FDA compliance tools — available to everyone, with no account or registration required. These tools are designed to help manufacturers, importers, and regulatory professionals work faster and stay compliant. Popular tools include:

• Cosmetic Drug Classifier — instantly verify whether your product is a cosmetic or drug
• Cosmetic Registration Navigator — helps you to decide whether your cosmetics need registration
• FDA Fee Estimator — get an instant cost estimate for FDA registration
• Food Label Scanner — find out if your food product label complies with FDA regulations
• MoCRA Product Code Builder — generate MoCRA product code instantly
• OMUFA Fee Navigator — determine whether your establishment needs to pay OMUFA fees

Explore all free FDA compliance tools →

Proprietary Tools and Platforms

Beyond consulting and free tools, LMG has developed professional-grade platforms that help manage complex FDA submissions and ongoing compliance:

LMG SPL Matrix™

A structured product labeling (SPL) tool purpose-built for FDA drug listing, Drug establishment registration, NDC labeler code request, and GDUFA self-identification submissions. LMG SPL Matrix™ simplifies the preparation and validation of SPL files, reducing errors and submission turnaround time.

LMG eCTD Pro™

Electronic Common Technical Document (eCTD) preparation and submission support for FDA drug submissions — with a primary focus on Drug Master File (DMF) submissions, including DMF annual reports and amendments. LMG eCTD Pro™ also supports NDA, ANDA, IND, and related applications, helping clients meet FDA’s electronic submission requirements accurately and on time.

LMG Compliance Monitor™

An ongoing compliance monitoring platform that conducts daily scans of the FDA Import Red List (DWPE) and the OMUFA fee arrears list — so nothing slips through the cracks. If your firm appears on either list, we’re notified instantly, verify the finding, and alert you directly. Every alert is human-verified by our U.S.-based team, and the service is complimentary for LMG clients. Particularly useful for companies managing multiple products and facilities.

FDA Detention and DWPE Red List Removal

If your facility or products are on the FDA’s Detention Without Physical Examination (DWPE) list — commonly known as the Red List — every shipment you send to the United States faces automatic detention at the port of entry. This is one of the most urgent and damaging compliance situations a foreign manufacturer or importer can face.

LMG provides specialist assistance with FDA detention and DWPE Red List removal. We analyze the underlying compliance issues, prepare the required documentation and corrective-action evidence, and manage the submission to FDA to get your shipments released and your facility removed from the list.

If you are currently facing import detention, time matters — contact LMG immediately for a prioritized assessment.

LMG FDARegWatch — Complimentary FDA Registration Monitoring

Keeping your FDA food facility registration active is critical — a canceled or invalidated registration means your shipments face immediate detention at the U.S. port of entry. Yet the FDA sends no cancellation notices, so most companies only find out when a shipment is already held at the border.

LMG FDARegWatch is a complimentary, hands-on registration monitoring service available exclusively to LMG food facility clients. Our regulatory team proactively tracks the status of your FDA food facility registration and alerts you the moment a problem is detected — giving you time to resolve it before your next shipment is affected. As your U.S. FDA Agent, LMG can also act on your behalf immediately when an issue arises.

There are no additional fees and no separate enrollment. LMG FDARegWatch is built directly into your LMG client relationship.

Learn more about LMG FDARegWatch →

Why Clients Choose LMG

• Globally recognized FDA, CE Marking, and ISO consulting firm since 2009
• 15,000+ projects successfully completed — FDA registrations, 510(k)s, listings, and label reviews
• Headquarters in Aurora, Illinois, USA, with associates worldwide
• Price-lock stability since 2009 — no fee increases, no hourly consulting, no hidden charges
• All prices are published transparently on the LMG website
• Full range of services: registration, US FDA Agent, label review, submissions, renewals
• Free FDA registration certificate issued with every registration
• Serving clients in 150+ countries across all FDA-regulated product categories
• Suite of free FDA compliance tools — no account required
• Proprietary platforms: LMG SPL Matrix™,  LMG eCTD Pro™, and  LMG Compliance Monitor™
• Specialist FDA detention and DWPE removal assistance
• Complimentary LMG FDARegWatch registration monitoring — exclusive to LMG food facility clients