05.25.23 -- All You Need To Know About Contamination Control Strategies, Part 1

Discover how a biopharmaceutical company can de-risk the launch process by choosing a suitable autoinjector technology and partner.

This article describes the advantages of a system that can streamline the tech transfer process by enabling efficient drug development activities and process data collection.

Inspection technologies play a crucial role in ensuring the safety, quality, and reliability of tablet and capsule packaging. Explore package integrity testing methods proven to be accurate and efficient.

Discover a streamlined process that delivers complete custom cleanrooms from scratch in as little as four months from concept initiation.

Pharmaceutical manufacturing staff, equipment, and premises are all subject to stringent quality controls. Read more about the latest status, trends, and technologies in parenteral filling equipment.

A variety of concerns — underscored by supply chain disruptions driven by the COVID-19 pandemic — are pushing companies to redraw global supply chains to resume more domestic manufacturing.

For peptide APIs, using a liquid-phase peptide synthesis (LPPS) approach offers a cost-effective process for large-scale manufacture by eliminating the need for specialized equipment and excess raw materials.

For parcel processing, as well as food and healthcare packaging, recent technology advancements have made in-motion weighing operations more precise and profitable.

We give an overview on the theory of scaling, present workflows and strategies, discuss which data are needed for successful scaling, and present case studies that use a web-based scaling tool.

A CDMO was looking to solve the issue of charging sterile drug substances into a mixing tank, which is a widespread problem in aseptic processing and particularly in formulation. 

A pharmaceutical manufacturer sought a mixing solution to successfully disperse the active ingredient finely enough so that the suspension remained stable, didn’t separate over time, and was not over-sheared.

Examine the first commercial live shipment of temperature-critical autologous final CAR-T drug product from a U.S. manufacturing site to a hospital in Japan.

The pros and cons of soluble and insoluble processes: isolating, solubilizing, and properly refolding, and strategies to improve the performance of IB processes.