Pharmaceutical Technology’s Pharma Knowledge Resources Newsletter:
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PharmTech
November 2017
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In This Issue

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

FEATURED WHITEPAPER

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.

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Formulation

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.

Oral Dose Film-Coating System Case Study

Roquette

ReadiLYCOAT® is a breakthrough in film-coating for heat-sensitive products. Download our case study which demonstrates how ReadiLYCOAT® offers a practical solution for tablet film-coating at low bed temperature.

Roquette Taste-Masking Technology Case Study

Roquette

Download the case study and learn more on how Roquette’s taste-masking technology KLEPTOSE® Linecaps (KL) allows the delivery of an efficient taste-masking solution with total safety.

Manufacturing

How to Source Pneumatic Conveying Systems for Pharmaceutical Excipients, APIs, and Other Powders that are "Difficult-to-Move"

David Kennedy; Vac-U-Max

This technical paper addresses key topics and design trends to consider when designing a sanitary pneumatic conveying system for batch and continuous processes. This application note defines difficult powders and their respective poor-flow properties, addressing the challenges in moving these powders into the conveying line from the pick-up point, feeding excipients and APIs at a constant rate, and discharging material to from the material receiver, while maintaining a dust-free processing environment.

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.

Quality

Pharmaceutical Cleaning Validation

Malcolm McLaughlin; Alconox, Inc.

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

Your Guide to Better Employee Training

Tim Lozier; EtQ

Download this whitepaper to learn how an automated Training Management System allows organizations to manage and track training events within the organization.

LabVantage and 21 CFR Part 11/Annex 11 Compliance

Jeff Vannest, Senior Director of Product Management; LabVantage

LabVantage outlines how its software solutions help pharmaceutical, medical device, and other regulated industries comply with two important data integrity standards. The paper, LabVantage and 21 CFR Part 11/Annex 11 Compliance: Understanding the Regulations and How LabVantage Successfully Helps Customers Comply with These Regulations, also addresses LabVantage’s approach to anticipated guidance on temporary data.

Outsourcing

Outsource or In-House? The Evolving Role of Analytical Services in Pharmaceutical Manufacturing

Impact Analytical

Analytical services have become a “make-versus-buy” decision; pressures within the current economic environment are prompting some companies to develop a new perspective on which capabilities remain “core competencies,” and which can be outsourced to reduce expenses.

Supply Chain

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.

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