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Whether you're sourcing components, evaluating equipment, or just exploring what MIS can do — we'd love to hear from you.
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Frequently Asked Questions
What types of companies does MIS work with?
MIS works with medical device OEMs, contract manufacturers, start-up companies, and R&D teams across the US. We support companies at all stages — from early development through commercial-scale production.
How does the sourcing process work?
We begin with a requirements discussion — specifications, regulatory requirements, volume, and timeline. We then connect you with qualified suppliers from our network and provide technical support throughout the qualification and procurement process.
Can MIS help with regulatory/quality requirements?
While MIS is not a regulatory consulting firm, we understand FDA/ISO requirements affecting manufacturing and can help connect you with suppliers whose processes and quality systems align with your regulatory needs. We can also refer you to specialist regulatory consultants when needed.
What is the typical timeline for a sourcing engagement?
It depends on the project complexity. Simple sourcing requests can yield supplier introductions within days. More complex engagements involving custom components, equipment specifications, or process development may take several weeks. We'll align expectations at the outset.
Does MIS work with companies outside the US?
Our primary focus is the US medical device market. However, we do work with international companies that are seeking US-based manufacturers, equipment suppliers, or technical expertise. Contact us to discuss your specific situation.