Co-micronization is a powerful strategy to improve uniformity, dispersion, and bioavailability of pharmaceutical blends. At Munit, we perform GMP-certified co-micronization of APIs and excipients using high-performance spiral jet mills in controlled environments.
What Is API Co-Micronization?
Co-micronization involves the simultaneous micronization of two or more components, such as an API with a carrier or excipient. This enhances homogeneity and surface interaction, particularly in inhalation, topical, and low-dose formulations.
GMP-Compliant Processes and Documentation
Each co-micronization process at Munit follows validated GMP protocols. Our workflows include dedicated batch records, equipment cleaning validation, and analytical testing for particle size distribution and homogeneity.
Technical Capabilities and Applications
We offer dry powder co-micronization inside isolators or open systems depending on the compound’s OEB classification. Our process is ideal for steroids, cytotoxic APIs, and inhalable blends where uniform particle size is essential.
Why Choose Munit for Co-Micronization?
With in-house engineering, flexible setups, and over 60 years of experience, Munit delivers tailored co-micronization services that scale from lab to production with full traceability and regulatory compliance.
Improve API performance through co-micronization.
Contact Munit for a custom co-micronization solution.