Decades of Expertise
in Inhaler Assembly

From low-volume lab-scale setups to high-capacity production lines, Mikron ensures consistency in processes and precision in outcomes. Key capabilities within our metered dose and dry powder inhaler manufacturing process include: plastic gears assembly, dose counter assembly, canister testing and handling, strip slitting, coiling and insertion, Vision quality control, X-ray testing, leak and functional testing, Pharma code management and laser marking Data Matrix code —all up to 180 parts per minute. 

Our Pre-Production services provide end-to-end support, including design for manufacturability/assembly (DFM/DFA), process optimization, and Proof of Principle—all compliant with FDA, GMP, and GAMP 5 standards. Additionally, our Denver facility enables small-batch assembly production for non-commercial devices in a cleanroom setting. For regulatory submission samples, our Mikron MAIA and Mikron MiniCell offer efficient, repeatable assembly processes. If your inhaler device is in the development stage, our Pre-Production services can guide you to a successful launch with minimized risks, supported by our advanced engineering capabilities.

With a global footprint, Mikron Automation provides seamless support, from initial engineering consultations to high-volume production and ongoing asset maintenance. Partner with us to innovate and achieve excellence in inhaler manufacturing.