Compliance Auditing

LexaMed offers a full spectrum of focused Domestic and International Compliance Audits which include, but are not limited to:

  • System GAP Analysis for compliance with US and International statutory requirements, ISO standards and industry guidelines
  • Pre-PAI Preparedness
  • Pre-FDA GMP Preparedness
  • Pre-ISO Certification
  • Vendor / Supplier Qualification / Re-Qualification
  • Internal Corporate Compliance


LexaMed has state of the art, integrated Laboratory, Research and Consulting capabilities and is uniquely qualified to assist with post-audit verification activities which include, but are not limited to:

  • Generation and Management of Compliance Action Plans
  • Assistance with Execution of Remediation Activities
  • 483 and Warning Letter Responses
  • Post-Audit Sustainable Compliance Evaluations

Need a Quick Quote?

We have several experienced, certified auditors on our staff with various areas of expertise.  If you would like to schedule an audit, please email your specific request, including name, company name, and desired time frame to

Medical Device and Pharmaceutical Manufacturing Operational Audits

LexaMed is an internationally recognized industry leader at performing Medical Device and Pharmaceutical Manufacturing Operational audits. Our experienced team of auditors and subject matter experts are eager to work with your company to provide a comprehensive assessment of all aspects of your facilities, quality systems and suppliers. Your company will benefit from the safety and confidence gained by our comprehensive, “eye of the agency” evaluations. Contact LexaMed to discuss our specialized auditing capabilities which include, but are not limited to:


  • Pharmaceutical cGMP: 21 CFR Parts 210/211
  • IPEC-PQC Excipient cGMP
  • Non-Sterile Solid Dosage
  • Large and Small Volume Parenteral
  • Isolator Technology
  • Terminal Sterilization
  • Aseptic Operations

Medical Device

  • Medical Device CFR: 21 CFR Part 820
  • Quality Systems ISO 9001 and 13485
  • Canada MDR (Medical Device Regulations)


  • All Sterilization Techniques
  • Parametric Release


  • Dietary Supplements cGMP: 21 CFR Part 111


  • Laboratory GLP: 21 CFR 58, ISO 17025


  • Computer Systems & Electronic Records, Part 11


  • Equipment, Process and Method Validation