API Micronization in GMP Cleanroom Facilities

Munit operates state-of-the-art cleanrooms and high-containment isolators dedicated to API micronization. Our infrastructure ensures full GMP compliance, environmental control, and operator safety during powder processing.

Cleanroom Classifications and Zones

We offer multiple cleanroom grades (ISO 8 to ISO 5), including:

  • Dedicated micronization rooms
  • Airlocks and material pass-throughs
  • Zoning for high-potency APIs

All rooms are monitored for particulates, temperature, humidity, and pressure differentials.

Containment for HPAPI and Cytotoxics

High-risk materials are processed in OEB5 isolators inside classified rooms. Equipment is configured for dust-free transfer, HEPA filtration, and inert conditions, supporting a wide range of APIs.

Cleaning Validation and Documentation

Each batch is supported by:

  • Environmental monitoring reports
  • Cleaning validation protocols
  • GMP batch records and traceability logs

Our facilities are routinely audited and qualified by regulatory agencies and clients.

Process your APIs in world-class cleanroom environments.
Schedule a facility tour or virtual audit with Munit.