Terriva supports pharmaceutical manufacturers worldwide with powder processing, blending, containment and compliance-led solutions — engineered for GMP environments and trusted across 50+ countries.
From R&D-scale blenders to fully integrated production suites, every Terriva system is engineered for the precision, compliance and batch consistency that pharmaceutical manufacturing demands.
Pharmatech
Containment Systems
GAMP-aligned, GxP-aware, 21 CFR Part 11-ready, ATEX-rated. Compliance is the foundation of every Terriva system — designed in, not bolted on.
Equipment engineered to deliver consistent results batch after batch, across decades. Many Terriva systems are still running flawlessly thirty years after installation.
Containment, interlocks, ATEX-rated equipment and operator-led design — protecting the people who run your production lines, every shift.
Forty years focused on powder behaviour, blending dynamics and containment integrity. We are specialists, not generalists.
Controls & software
Terriva’s controls and software upgrades modernise existing powder processing equipment — improving usability, supporting 21 CFR Part 11 compliance, and extending equipment life without the cost of full replacement.
New PLC architecture, current-generation HMI.
Modern batch controls, recipe management.
Audit trails, e-signatures, role-based access.
Scoping, validation pathway planning.
GET IN TOUCH
Whether you’re specifying a new system, modernising existing equipment or reordering consumables — our team will help you identify the right solution.
