Global Leaders in Powder Processing for Pharmaceutical Manufacturing.

Terriva supports pharmaceutical manufacturers worldwide with powder processing, blending, containment and compliance-led solutions — engineered for GMP environments and trusted across 50+ countries.

Trusted by leading pharma manufacturers worldwide

Forty years of pharmaceutical powder processing specialism.


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

Powder blending solutions for pharma manufacturing.

Bespoke and standard blending systems built to GMP standards — scalable from R&D-scale benchtop units through to full production manufacturing. Engineered to a standard that meets pharma’s exacting demands.

Containment Systems

Keep the powder where it belongs. Without worry.

Drums, vessels and consumables for safe, dust-free containment, transfer and handling — engineered to protect operators, product and compliance across every stage of pharmaceutical manufacturing.

Why pharmaceutical manufacturers choose Terriva


Built for regulated environments

GAMP-aligned, GxP-aware, 21 CFR Part 11-ready, ATEX-rated. Compliance is the foundation of every Terriva system — designed in, not bolted on.

Reliable performance

Equipment engineered to deliver consistent results batch after batch, across decades. Many Terriva systems are still running flawlessly thirty years after installation.

Operator safety

Containment, interlocks, ATEX-rated equipment and operator-led design — protecting the people who run your production lines, every shift.

Powder processing specialists

Forty years focused on powder behaviour, blending dynamics and containment integrity. We are specialists, not generalists.

Controls & software


Modernise existing equipment for modern pharmaceutical manufacturing.

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.

Control upgrades

New PLC architecture, current-generation HMI.

Software upgrades

Modern batch controls, recipe management.

21 CFR Part 11

Audit trails, e-signatures, role-based access.

Applications Support

Scoping, validation pathway planning.

Operating in a regulated environment? You're in the right place.

GAMP & GxP

GAMP & GxP

Supporting regulated pharmaceutical manufacturing environments where process control, traceability and validation are critical.
21 CFR Part 11

21 CFR Part 11

Audit trails, electronic records, validated e-signatures and data integrity for FDA-regulated manufacturing.
ATEX

ATEX

Safe, compliant blending in explosive-risk areas — engineered for Zone 1, 2, 21 and 22 environments.

GET IN TOUCH


Talk to a powder processing specialist.

Whether you’re specifying a new system, modernising existing equipment or reordering consumables — our team will help you identify the right solution.

Home
This website uses cookies to improve your experience. By using this website you agree to our Data Protection Policy.
Read more