ISO 9001:2015 registered
Quality management discipline supports repeatable manufacturing, corrective action, documentation, and customer-focused process control.
Quality and certifications
<p>Quality registration, IPC workmanship expectations, lead-free capability, controlled goods awareness, and documented process discipline support MIS manufacturing work.</p>
Quality foundation
MIS combines registered quality systems, recognized workmanship standards, documented controls, and disciplined manufacturing practices to support dependable electronics production.
Quality management discipline supports repeatable manufacturing, corrective action, documentation, and customer-focused process control.
Medical device quality registration supports customers that need tighter documentation, controlled processes, and regulated manufacturing expectations.
Printed circuit assembly standards such as IPC-A-610 help guide workmanship, inspection, acceptance criteria, and quality practices across MIS manufacturing programs.
Lead-free process capability supports modern environmental and customer compliance requirements for electronic assemblies.
Controlled Goods registration supports responsible handling expectations for eligible Canadian Military/Aerospace and sensitive customer programs.
Participation in the Surface Mount Technology Association connects MIS with electronics-assembly education, industry practice, and technical development.
ISO 9001:2015 and ISO 13485:2016 are quality-management-system registrations. IPC and SMTA connect the team with electronics workmanship and industry practice. Lead-free capability, ESD controls, and Controlled Goods registration address different manufacturing or program requirements.
Review the evidence relevant to your program and confirm the current certificate scope, customer requirements, and acceptance criteria with MIS before release.
ISO 9001:2015 and ISO 13485:2016 are quality-management-system registrations. IPC and SMTA connect the team with electronics workmanship and industry practice. Lead-free capability, ESD controls, and Controlled Goods registration address different manufacturing or program requirements.
View the MIS certificate evidence for ISO 9001, ISO 13485, IPC, SMTA, Controlled Goods, and lead-free manufacturing.
Registrations and standards provide a foundation. Each customer program can still require its own drawings, acceptance criteria, traceability, inspection level, functional test plan, records, regulatory notes, and delivery expectations. Share those details early so MIS can confirm what applies to the build.
MIS maintains commercial, quality, ordering, and supplier guidance that supports clearer expectations on both sides of the manufacturing relationship.
Request the latest applicable revision from MIS before relying on a controlled document for an order, supplier response, or quality decision.
Commercial terms for customers working with MIS.
Purchasing conditions governing supplier transactions.
The company commitment to customer requirements, continual improvement, and employee responsibility for quality.
A broader summary of engineering, manufacturing, quality, supply-chain, project-management, and test capabilities.
Information customers can use to prepare a clearer, more complete PCB order package.
Quality, traceability, corrective-action, and compliance expectations for MIS suppliers.
Next step
Share the standards, inspections, records, and testing expectations that matter to your assembly.