Build your pharma development and manufacturing knowledge base with the latest whitepapers, application notes, posters, and other educational resources from bio/pharma industry suppliers.

Effect of Extrusion Parameters on Solid Dispersions

C. Martin, J. DiNunzio, J.M. Keen, A. Machado, J.W. McGinity, H. Sandhu; Leistritz

The objective of this research is to investigate the extrusion process space in co-rotating and counter-rotating extruders, which is critical in ensuring the properties of pharmaceutical solid dispersions.

Pharmaceutical Cleaning Validation

Malcolm McLaughlin; Alconox

A comprehensive description of how to perform cleaning validations in the pharmaceutical industry. This paper focuses on the calculations as well as the process.

How Quality Data Can Impact Company-Wide Performance

Jaseem Mahmmdla senior product manager, Mike Edwards senior product manager; Sparta Systems

In this paper, we examine key factors driving manufacturers toward a more holistic form of quality management, and provide a new data model that companies can use as part of their quality management systems (QMS) to more easily create meaningful business insights that help the organization as a whole.

The Risk Management Guidebook

Brenda Percy; EtQ

This guidebook brings you risk management tools and strategies, how to integrate risk into standards and processes, and fun takes on risk management.

Simple Steps to Speed Encapsulated Drug Development

Capsugel – Now a Lonza Company

In the pharmaceutical industry, speed to market is essential for gaining a competitive position. New encapsulation technologies now make it possible to streamline research and development activities, improve product development, and jump-start time to market.

TruTag Technologies and Colorcon Stability Study

Michael O’Neill, chief science officer; TruTag Technologies

This whitepaper presents a study undertaken by TruTag Technologies and their technical collaborator, Colorcon, and demonstrates that the application of TruTag^® microtags has no impact on the drug release, assay, or appearance of pharmaceutical tablets after exposure to accelerated storage conditions.

Overcoming Resistance and Migrating to Content Automation

Ray Glemser, PhD; Glemser Technologies

Automation can help organizations in the life sciences streamline a content delivery process that may already be strained by quality controls, limited resources, or compliance issues.