ISO 9001 Certification

Guaranteed Certification

Fast Processing

Lowest Fees

ISO 13485 Certification

Integrated Quality System for

ISO 13485 & 21 CFR 820

Quality Manual


Medical Device CE Marking

Clinical Evaluation

Technical File

US FDA Registration

Free Registration Certificate

US FDA Agent service

Label Compliance

US FDA Inspection

GMP Compliance Help

FDA 483 Assistance

GAP Analysis

Third Party Inspection

Inspection for product quality

Process quality inspection

Pre-shipment Inspection

Welcome to Liberty Management Group Ltd. (LMG)

Liberty Management Group Ltd. (LMG) is an ISO 9001 Certified company headquartered at Aurora, Illinois, USA, with offices and associates around the globe. LMG was established in the year 2009 to assist domestic and foreign establishments in US FDA Regulations; and extends its service to ISO 9001, ISO 13485, and CE Marking.

ISO 9001 : 2015 Certification - Chicago

ISO 9001 : 2015 is a globally accepted standard for quality system certification, which can be used in any organization, small or large; any industry, manufacturing or service. Large and Medium size organizations in manufacturing and service industry, always request ISO 9001 Certificate to their suppliers / contract manufacturers. By requesting ISO Certificate these organizations can make sure their suppliers are complying with ISO Standards and have minimum required quality for their products and services. ISO 9001 implementation require frequent site visit, so it is advisable to find an ISO consultant from your home town. We help organizations (manufacturing and service) in Chicago and suburbs to achieve ISO 9001 Certification. Our experienced consultants can help you in ISO 9001:2015 transition from ISO 9001:2008.

US FDA Registration

US FDA regulates products marketed in the USA, such as Food, Drug, Medical Device, Radiation-Emitting, Cosmetics, Biologics, dietary supplements, animal foods etc.

LMG provide US FDA Registration services around the globe, our service includes, FDA registration, US FDA Agent service, Label review, Drug listing, medical device listing, UDI Submission, NDC Labeler code request, GMP, 21 CFR 820 quality system regulations etc. we provide free registration certificate after completing each registration.

CE Marking

CE-Marking (CE Mark) is a mandatory requirement for marketing certain products like Medical devices in the Europe. CE marking declare that the products meets the EC Directives. We assist US Medical device companies to get CE Marking, our services include, technical file preparation, review clinical evaluation report (CER), ISO 13485 implementation, Notified body co-ordination, notified body audit support, biocompatibility testing etc.

Third party inspection

LMG provide Third party inspection service to manufacturing and trading industry, our expertise includes food, drug, medical device, cosmetic, coir, Rubber and latex dipped goods industry.

US FDA inspection

Assistance with GMP Compliance, GAP analysis, Quality Manual and Quality System Procedures. LMG also help with FDA 483 warning letter.

LMG has built strong relationships with major consultants and consulting groups; each associate has special expertise in their respective field and a wide network. These expertise and network helps us to provide you high quality, cost-effective services in a minimum time frame.

Our Consulting Services includes

For more information, Please contact us with detailed information.