Medical Device Engineering and Development Services
Accelerate your path to market with Sanner’s end-to-end medical device design and development services.
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Accelerate your path to market with Sanner’s end-to-end medical device design and development services.
Sanner takes medical and drug delivery devices from early concept through design transfer and into production, with the development and manufacturing all under one roof.
Our engineers have developed hundreds of medical devices and combination products, spanning advanced diagnostics, wearable and portable devices, and custom single-use drug delivery systems. With more than 150 engineers worldwide, our team works through a unified product development process aligned with human-centered design and regulatory support.
From completing verification and validation to scale-up process optimizations in the plant, you’re supported through every milestone by the same Sanner development team.
Design for Manufacturing and Assembly (DFMA) is built into our development process from day one. With several decades of injection molding experience, our manufacturing teams weigh in during development, not after, so tooling and production cost are designed down rather than engineered out later.
DFMA methodology extends to your supply chain. Material selection, component count, and sourcing decisions all shape how exposed your program is to lead times and sourcing risk. We factor those in during design, and with molding, assembly, and packaging in-house across our manufacturing sites, more of your bill of materials stays under our control.
We put design centers where our clients are, from coast to coast in the United States to the UK and Germany. That proximity means working sessions, design reviews, and build support happen in person when they need to.
Each Sanner design center is integrated with our manufacturing sites, giving your program access to tooling, molding, and process engineering input throughout development.
The highly motivated personnel assigned to the project were very well trained and showed high levels of expertise. For specific aspects, trained experts from within the organization were allocated to the project.
Design transfer is where most programs lose time. Our dedicated transfer team and process engineers are involved before the design is finalized, so the move from verified design to validated production line is planned rather than improvised.
Equivalent quality systems operate across every Sanner site, so a program developed in one region can be manufactured in another without rebuilding the quality framework.
End-to-end development and manufacturing for an innovative anesthetic spray.
Robust development of a next generation platform autoinjector.
Developing a connected syringe accessory that makes the smallest doses measurable.
