Direct API Capsule Filling: A Faster Path to Market
Direct filling of pure active pharmaceutical ingredients (APIs) into capsules can significantly shorten capsule development, and manufacturing processes as well, by avoiding complex formulation and blending steps. As a result, pharmaceutical companies can accelerate product development and achieve earlier market entry.
Anastasios Chrisogiannis
Sales Manager - Capsule Filling and Weighing
Single-Use Containment for High-Potency OSD Manufacturing
Discover how single-use containment solutions are transforming high-potency OSD manufacturing by improving containment performance, accelerating scale-up, and lowering total cost of ownership. This session highlights the advantages of DoverPac® and Flexible Enclosures in supporting safe, efficient, and flexible pharmaceutical production.
Suresh Swaminathan
General Manager, Single-Use Containment
Luis Santos
Product Specialist
Tablet Design Optimization to Prevent Medication Errors
Having a unique tablet for your product is a critical component of consumer health to prevent medication errors. This presentation addresses optimization techniques in relation to font, scale, color, shadow definition, engraving details, pre-picking, and film coating.
Todd Martin
Senior Technical Service Engineer
The Qwv-150: Full-Surface Capsule Inspection and Weight Sorting in One Unit
Discover the new Qwv-150, Qualicaps' latest scale-up model that combines full-surface capsule inspection and weight sorting in a single compact unit. Building on the proven usability and precision of the Qwv-100, the Qwv-150 delivers up to 150,000 capsules per hour and now complies with both 21 CFR Part 11 and CE standards.
Qualicaps' presentation will highlight how the system addresses labor shortages, boosts productivity, and ensures consistent global manufacturing quality.
Dennis Johnston
Equipment Technical Services
Built-In GxP Capabilities for eBR, Logbooks, and Line Clearance
Every manufacturing operation is unique and dynamic, and off-the-shelf and one-time digitalization efforts fall short in GxP environments. Learn how built-in GxP capabilities (electronic signatures, audit trails, automatic attributability, review by exception) and a composable platform support eBR, logbooks, line clearance, and lab operations.
Matt Deffenbaugh
Pre Sales Engineer
Abstracts from the remaining exhibitors are still coming in and are posted here as they arrive.