We want to build the world’s leading solution provider for pharmaceutical micronization through a focused and high quality service portfolio, long-term client relationships, innovative technologies and highly skilled employees.


Our business is focused on mechanically improving the physical properties of APIs to be the best-in-class partner for pharmaceutical and fine chemical customers worldwide. In delivering our solutions, we combine our experience in production, engineering and analytical know-how.


Our micronization sites are full cGMP compliant and regularly inspected by FDA and Swissmedic and certified by the Japanese Health Authorities.


Our capacity is more than 1000 MT per year with 36 available mills covering various technologies.

The Quality Policy of Engineering Operations Division can be provided on request.


Micromacinazione commitment to excellence is guaranteed by the continuous improvement of our Quality Systems . Over the last 10 years, our facilities have been inspected by more than 200 different auditing teams. The regular customer, regulatory and internal audits further contribute to assure compliance with the GMP requirements.