We help you refine your innovative idea and assess its feasibility so that you can confidently move forward with a clear, market-ready concept.
We optimize your product design with end users in mind so that you can reduce production costs, streamline development, and ensure scalability.
We guide you through our Design for Manufacturing (DFM) and regulatory compliance process so that your device meets industry standards and is ready for market approval.
We help you refine your innovative idea and assess its feasibility so that you can confidently move forward with a clear, market-ready concept.
Patrick has worked with industry leaders like Medtronic, Boston Scientific, and Johnson & Johnson, understands what it takes to bring a device to market efficiently while avoiding costly missteps.
With over 15 years in medical device design, manufacturing, and supply chain management, he helps early-stage startups, founders, and inventors navigate the complex journey from idea to full-scale production.
He is an experienced medical device engineer, not a consultant. He embeds himself in your product development team as a 𝗚𝗿𝗼𝘄𝘁𝗵 𝗣𝗮𝗿𝘁𝗻𝗲𝗿, providing leadership, program management, and mentorship while bringing your market-disrupting product to life.
When you’re ready for manufacturing, he’ll stay with your team, continuing to provide guidance and leadership as your project moves into commercialization.
Streamlined development, no costly redesigns
Ensure device is manufacturable + cost effective from the start
Reduced sourcing risks, faster production
Compliance-first approach, minimize approval delays
Integrated prototyping & validation for efficiency
Smoother path to secure funding, attract buyers, full-scale production
Mitigate production risks, long-term cost savings
Avoid pitfalls, done-for-you implementation
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