Newsletter | September 26, 2025

09.26.25 -- Lean Manufacturing Implementation In Pharmaceutical Injectable Facilities

SPONSOR

Webinar: Inside the Barrier: Optimizing Aseptic Processing with Isolator Technology

Protecting patients starts with sterility assurance—and pharmaceutical isolators deliver unmatched safety, compliance, and efficiency. Join Germfree experts Forrest Brown and Brandon Serle for an inside look at cutting-edge isolator design and real-world applications. Discover how isolators streamline operations, meet evolving regulations, and integrate with modular facilities to scale reliably. Don't miss this opportunity to future-proof your sterile manufacturing strategy. Click here to learn more.

INDUSTRY INSIGHTS

Sustainability By Design In API Manufacturing

Explore the urgent need for sustainability in small molecule API manufacturing, as well as reveal regulatory drivers, green chemistry innovations, and practical strategies to reduce emissions.

Delving Into Modular Cleanroom Designs For Drug Manufacturing

Uncover the reasoning behind the increasing demand for cleanroom technology, as well as the advantages modular cleanroom design brings to the sterile processing of complex therapies.

Scaling Up: Increasing Production Capacity While Reducing Costs

Medical device companies must meet the demand plan for their devices while managing production costs. Gain valuable insights for scaling up production capabilities efficiently and cost-effectively.

FEATURED EDITORIAL

Lean Manufacturing Implementation In Pharmaceutical Injectable Facilities

This comprehensive analysis examines lean manufacturing implementation challenges and evidence-based solutions derived from leading pharmaceutical organizations. 

INDUSTRY INSIGHTS CONTINUED

Pharma 4.0 And Digitalization Strategies For Drug Manufacturing

Examine a modular approach to Pharma 4.0 that empowers organizations to embrace digital transformation at their own pace and is tailored to their unique needs.

Leverage Apps To Reduce Line Changeover Time From 14 Days To 3

A global biopharma leader modernized its complex equipment changeover process using an innovative platform to achieve faster execution, fewer errors, and greater visibility through digitized SOPs.

Test Kit Management: Your Visual Inspection Program's Hidden Weak Point

A proper test kit management program is no longer a “nice-to-have”—it’s a compliance necessity. Without a structured system, you risk inspector drift, failed audits, and errors in batch release.

Clinical And Formulation Strategies For Targeted Peptide Drug Development

Novel technologies and therapies are helping drug developers to overcome challenges associated with the development of injectable and oral peptide formulations.

Understanding Modern Storage Tank Design And Fabrication

Industries rely on advanced storage tanks and pressure vessels to safely manage liquids, gases, and powders. Discover how custom-engineered solutions can enhance efficiency, safety, and compliance.

Experimental CCI — Induced Neuropathic Pain Model

Advance neuropathic pain research and therapeutic development with the Chronic Constriction Injury (CCI)-induced neuropathic pain model to uncover mechanisms and evaluate promising candidates.

Modular Facilities With Smaller Footprint Through Dynamic Perfusion

Learn how a top CDMO leveraged dynamic perfusion technology to boost biomanufacturing throughput, cut capital costs, and enable flexible, multi-modality production.

The Challenges Of Moving A Bioconjugate From Clinic To Market

Working with a partner that provides a one-stop shop for bioconjugate development and manufacturing helps prevent missteps that threaten the delivery of life-saving drugs to patients who need them.

Replacing Bleach In Removal Of DNA

Find out more about an effective cleaning solution that removes DNA from laboratory equipment and materials without the need for bleach.

Spray Drying For Innovative Dry Powder Inhaler Combination Formulations

Combination therapies delivered directly to the lung by dry powder inhalants are an effective means of reducing patient burden. Read about case studies that illustrate the potential for improving care.

Streamline Your Fill And Finish Process Of Ready-To-Use Cartridges

An optimized nest design for pre-fillable cartridges was designed using numerical simulation and data analytics to improve efficiency in pharmaceutical production.

SPONSOR

Webinar: Extrusion-Based ASD Scale-Up: Ensuring Performance Through Process Understanding

Boost your drug development success with Lonza’s upcoming webinar on amorphous solid dispersions (ASDs). Learn how hot melt extrusion (HME) can enhance bioavailability, cut costs, and scale efficiently—backed by real-world lab and pilot trials. Compare HME and spray drying while gaining exclusive insights into Lonza's advanced capabilities and proven expertise in ASD manufacturing. Don't miss it! Click here to learn more.

SOLUTIONS

Two Decades, One Focus: Sterile Manufacturing Excellence

Industry-Leading Differential Scanning Calorimeter

USP<1062> Tablet Compression Characterization

Transforming Drug Delivery. Transforming Lives.

A Solution For Batch Reporting And Data Analytics In Life Sciences

Pharmaceutical Labeling Systems For Vials

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