Newsletter | May 25, 2023

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

Featured Editorial
Industry Insights
De-Risking Biosimilar Development With A Clinically Validated And Commercially Proven Disposable Autoinjector

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

Bridging The Divide: Streamline The Process Development And Tech Transfer Process

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 For Tablets And Capsules Packaging

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.

Building Modular Cleanrooms For Pharma At Warp Speed

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

The Need For Flexible Aseptic Filling And Isolation Systems In Pharma

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.

Reshoring A Nation’s API And Pharmaceutical Production

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.

Peptide Synthesis: Delivering Cost-Effective Strategies

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.

A Guide To Weigh Cell Technologies For Pharma And Food Industries

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

Simplify Bioreactor Scale-Up And Scale-Down

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.

Selecting Sterile API Transfer Technologies

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. 

Mixing Technology Unrivaled In Dispersion Of Hormonal Active Ingredient

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.

Distribution Of The First Commercial CAR-T Therapy From U.S. To Japan

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.

Inclusion Bodies: Mother Nature's Help Or Hindrance?

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


Expert users of ICR (for Isolators Clean Rooms) culture media will discuss regulatory guidelines, media packaging/storage conditions/shelf life, limiting false readings, and partnering with the right media supplier. Register.

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