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About A.P. Lyon

Quality Systems and Regulatory Support for Regulated Manufacturers

Aaron Lyon, founder of A.P. Lyon, medical device regulatory affairs and quality consultant

Aaron Lyon, founder of A.P. Lyon, has more than 30 years of experience in product design and development and in developing large-scale global manufacturing operations. During his career, he has served as Senior Director of Regulatory Affairs, Director of International Quality Assurance, NPD Engineering Manager, and Director of Manufacturing. His extensive experience and drive to offer products and services that exceed customer expectations create a positive and challenging atmosphere for the A.P. Lyon team.

30+

Years of Experience

Aaron Lyon, Founder

45

Countries Served

650+

Product Experience

Expertise and Markets Served

A.P. Lyon has served medical device companies in 45 countries. Our customers benefit from our experience in medical device design and development, validation, and facility development. The team also has extensive experience managing and directing manufacturing facility relocation projects and has successfully transferred more than 650 products to new manufacturing sites around the globe.

 

Today A.P. Lyon offers four families of editable management system documents: ISO 13485 and FDA QMSR for medical devices, Dual-Standard ISO 9001 + ISO 13485, ISO 9001:2026 for manufacturers and their suppliers, and an ISO 22000 / FSSC 22000 food safety management system aligned to FDA 21 CFR 117. We also provide consulting for each of these standards.

Our Mission

Our mission is to give regulated manufacturers (medical device, manufacturing and food companies) the documents and expertise to build quality and food safety systems that work in practice and hold up in audits.

Discuss Your Next Project

Contact A.P. Lyon to discuss your quality system, food safety system or regulatory support needs.

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