MultiBlend MB1200A Powder Blender
Production-scale blending with integrated container handling.
A robust, high-capacity blender engineered for demanding production environments. Quick-change container system and integrated tilting mechanism reduce manual handling, improve operator safety and shorten cycle times between batches.
- Quick-change container system: development through to full production scale
- Integrated tilting lifts and returns containers automatically
- GMP-compliant for hygienic, fully validated manufacturing
Designed for GMP-compliant manufacturing, the MB1200A maintains the highest standards of quality and hygiene while adapting to the changing demands of modern powder processing. For regulated environments, ATEX-rated and 21 CFR Part 11-ready configurations are available — supporting safe operation in explosive atmospheres and FDA-compliant electronic records for full audit traceability.
Benefits & uses
Production-scale capacity
Built for demanding production environments.
Quick-change container system
Handles small development batches and large production vessels on one machine.
Reduced manual handling
Integrated tilting mechanism lifts containers directly from trolley or pallet.
Improved operator safety
Automated lift and return reduces lifting risk.
Time savings
Quick container changes shorten cycle times between batches.
GMP-compliant
Built for hygienic, fully compliant production.
Typical applications
- Full-scale production
- Multi-batch operations requiring fast container changeovers
- Integrated production lines
- ATEX-rated versions available for explosive-atmosphere environments
- 21 CFR Part 11-ready configurations for FDA-regulated electronic records
Technical specifications
| Configuration | Production-scale blender with integrated tilting |
| Container system | Quick-change, accommodates small development through to large production vessels |
| Handling | Automated lift from trolley/pallet, blend, and return |
| Compliance | GMP-compliant manufacturing |
Why the Pharmatech MultiBlend MB1200A
GAMP-aligned engineering
Where required, the MB1200A can be specified and validated in line with GAMP risk-based principles for automated and computerised production systems in regulated pharmaceutical manufacturing.
Learn more about GAMP & GxP
GxP-ready by design
Engineered for the controlled, traceable, validation-ready environment that pharmaceutical manufacturing demands. GMP-compliant construction, integrated tilting mechanism with full safety interlocks, and quick-change container system support hygienic, fully validated production.
Learn more about GAMP & GxP
21 CFR Part 11 capable
Production-scale control systems can be specified with audit trails, electronic signatures and role-based access for FDA-regulated electronic records — purpose-built for high-throughput regulated manufacturing.
Learn more about 21 CFR Part 11
Data integrity supported
ALCOA+ principles supported through validated electronic records, secure data capture and reliable archival — keeping production-scale batch records inspection-ready throughout the equipment lifecycle.
Learn more about Controls & Software
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