The Four Pillars of ICH Q10
Author: Tim Lozier
Sponsored By: EtQ, Inc.
In this white paper, learn about the basics of the ICH Q10 model, the four pillars of ICH Q10, and how to apply them within your organization.

New Webcast: Understanding USP 36
Sponsored By: Vaisala
Please enjoy this 30-minute webcast from Mary G. Foster, PharmD., chair of the USP Expert Committee with Vaisala's senior regulatory compliance expert Paul Daniel as they review changes to the latest revision of USP <1079> and forthcoming changes to GDP.

Foaming via Melt Extrusion for Improving the Grindability of Extrudates and Dissolution Rate of Oral Dosages
Authors: G. Terife, C. Martin, C. G. Gogos, and N. Ioannidis
Sponsored By: Leistritz
Significant development efforts are occurring that utilize twin-screw extruder (TSE) technologies as part of unique foam extrusion systems for emerging bioplastics and pharmaceutical products.

Choosing the Right Hand Protection when Working with Chemotherapy Drugs
Sponsored By: Ansell Protective Products
This white paper explores what workers and employers should be concerned with when selecting hand protection for industrial life science applications.

Advanced Aseptic Liquid Processing Technology
Sponsored By: Weiler Engineering, Inc.
Weiler Engineering, Inc.'s corporate focus is to provide advanced aseptic liquid processing technology through the application of customized ASEP-TECH® Blow/Fill/Seal machinery and services. Serving the pharmaceutical industry has been Weiler's core business for more than 50 years. Weiler focuses on the patient and strives to provide the safest sterile aseptic packaging process for pharmaceutical liquids. This concept is based on studying and implementing learned technological advances driven by science.

Cleaning Validation for Pharmaceutical Manufacturing
Author: Malcolm McLaughlin
Sponsored By: Alconox, Inc.
This paper outlines the basics of cleaning validation, as well as discusses the kinds of support services needed for critical cleaning products in order to optimize your cleaning validation process.