News, guides & case studies

Insights from Terriva

Explore latest news and industry expertise.

Dust Containment Systems

31 May 2026

What Is a Dust Cap Seal and Why Is It Essential in Pharma?

In pharmaceutical manufacturing, poorly controlled transfer points can compromise containment. Dust Cap Seals provide a reliable solution to reduce dust, support GMP compliance, and improve process consistency.

Distributors

31 May 2026

Strengthening Our North American Partnership with Process North America

Powder Blending

27 Apr 2026

Audit-Ready by Design: What CDMOs Miss About 21 CFR Part 11 in Equipment Selection

Data integrity ensures that information remains accurate, complete, and reliable throughout its lifecycle. In pharmaceutical manufacturing, the ALCOA+ principles define what good data looks like—ensuring it is attributable, legible, recorded in real time, original, and accurate for audit readiness and decision-making.

Contract Development and Manufacturing Organisations

24 Apr 2026

The Evolving Role of the CDMO: From Manufacturing Partner to Strategic, Consultative Leader

Powder Blending

19 Mar 2026

How to Validate a Powder Blending Process: IQ/OQ/PQ Explained

Powder Blending

13 Mar 2026

How to Justify New Blending Equipment to Leadership

Discover how to justify pharmaceutical powder blending equipment investment by clearly communicating operational constraints, regulatory benefits, and production improvements to leadership teams responsible for capital decisions.

Next steps

Want to find out more?

Reach out to a Terriva expert for a free consultation meeting.