Home/About Us
Compliance Expertise,
Grounded in Practice
Liberty Compliance Solutions is the regulatory compliance division of Liberty Management Group Ltd, operating from our Aurora office in Greater Chicago. We help manufacturers and importers meet the requirements that stand between their products and their markets.
- A division of Liberty Management Group Ltd — established 2009
- Aurora, IL · Greater Chicago
- Submission-ready documentation
- On-time delivery
A Focused Division of an Established Practice
Liberty Management Group Ltd was established in Illinois in 2009 to help manufacturers with CE Marking, US FDA regulations and ISO certification. Liberty Compliance Solutions brings that work together under one dedicated division.
The reasoning is simple. Regulatory compliance rewards depth. A team that works on European Directives, ISO management systems, FDA premarket notification and food import rules every day builds judgement that a generalist cannot — judgement about which standard actually applies, what a notified body will question, and where a submission is likely to stall.
Over more than fifteen years, Liberty Management Group has taken more than 50 medical devices through FDA 510(k) clearance, delivered upwards of 15,000 regulatory and quality projects, and supported manufacturers in over 150 countries. Liberty Compliance Solutions draws on that same bench of expertise.
We work with manufacturers placing products on the European market, medical device companies seeking FDA clearance, organisations building certified management systems, and US importers who need a Foreign Supplier Verification Program that survives an FDA inspection. Our clients are based across the United States and Canada, and we support companies worldwide that need access to these markets.
An Established Regulatory Practice
Liberty Compliance Solutions is the compliance division of Liberty Management Group Ltd, an FDA and international regulatory consultancy operating from Illinois since 2009. The figures below are Liberty Management Group’s.
Established
Founded in Illinois to support manufacturers with CE Marking, US FDA regulations and ISO certification.
510(k) Clearances
Medical device premarket notifications taken through to FDA clearance.
Projects Delivered
Regulatory and quality engagements completed across the group’s service lines.
Countries Served
Manufacturers and importers supported into US and European markets worldwide.
How We Work With Clients
Clarity First
Before any documentation is written, we establish exactly which rules apply to your product and market. Most compliance problems trace back to getting this wrong at the start.
Evidence That Holds Up
Technical files, management systems and submissions are built to withstand scrutiny from auditors, notified bodies and FDA reviewers.
Capability Transfer
We would rather leave your team able to maintain the system than dependent on us to renew it every year.
Need Help with Compliance?
Our experts are ready to help you navigate regulatory requirements and achieve your certification goals.
Experienced Experts
Hands-on experience in regulatory compliance and management systems.
Tailored Solutions
Solutions that fit your business, industry, and product requirements.
On-Time Delivery
Efficient and reliable service to help you meet your business deadlines.