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Other Consulting Services

LMG provides a full range of regulatory consulting services beyond FDA registration — including CE Marking, ISO 13485, ISO 9001, and GMP consulting.

CE MarkingISO 13485GMP ConsultingSince 2009

Additional FDA & Regulatory Consulting Services

Liberty Management Group provides a comprehensive range of regulatory consulting services to help manufacturers comply with US FDA regulations and international standards.

  • CE Marking consulting for medical devices entering the European market
  • ISO 13485 Quality Management System consulting and gap assessment
  • GMP gap assessment and consulting for 21 CFR Parts 210, 211, 820
  • FSMA compliance consulting — Preventive Controls, Produce Safety Rule
  • Label review for food, drug, cosmetic, and medical device products
  • FDA 483 response and Warning Letter remediation
  • Import alert assistance and detention resolution
  • Prior notice submission for food importers

Frequently Asked Questions

Common questions about FDA registration and other consulting services.
Yes. LMG provides CE Marking consulting for medical devices entering the European market.
LMG provides ISO 13485 QMSR consulting and gap assessments to help manufacturers prepare for certification.
LMG provides GMP gap assessments for drug (21 CFR Parts 210/211), medical device (21 CFR Part 820), food, and cosmetic manufacturing facilities.

Need Regulatory Consulting?

Contact LMG for a full range of FDA and international regulatory consulting services.

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