Our ISO certifications and ITAR & FDA registration represent our commitment to excellence
Quality is not confined to one department or team at MME group. Quality is instilled at every level of the company and is the cornerstone of all that we do. We hold ourselves accountable for product outcomes; accountability defines our culture.
You dictate quality measurement criteria. We work with the end result in mind and complete advanced planning and risk analysis. Along with your quality controls, we apply a tiered quality system appropriately designed to your program needs. We support standard qualification to full FDA validation.
Quality Management Systems
We are ISO 13485:2016, which is a specialized certification for medical component manufacturing, and are ITAR and FDA registered for adhering to U.S. export laws for government projects.
UL and CE Certifications
The UL (North America) and CE (European Union) certification organizations grant the distinctive UL and CE marks on products that have been evaluated and meet rigorous standards for safe operation.
UL and CE certifications are part-specific. MME group can file paperwork and obtain the certification on your company’s behalf.
• ISO 13485:2016
• ITAR M34528
• FDA 3006535109
Collaborative Product Qualification
• IQ, OQ, PQ Qualification and Validation
• Automotive PAPP
• Control Plan
• FMEA / PFMEA
• SPC Analysis
• Cpk / Ppk Analysis
• Supplier Quality Management
• Incoming Inspection
• Melt Flow Index Testing
• Pull Force Testing
• Moisture Testing
• In Process Inspection
• In Process Inspection Fixtures
• Non-destructive thickness checks
• Gage R&R
• Lot Traceability