Newsletter | June 6, 2025

06.06.25 -- Using Virtual Reality To Enhance Aseptic Contamination Control

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Webinar: Cleanroom Conceptual Design Paradigm: Converting Spaces for GMP Operations Part 2

Join the AES Cleanroom Technology webinar to explore cleanroom conceptual design strategies for GMP operations. Learn how to convert alternative spaces into efficient production facilities while minimizing capital risk. Discover key principles for integrating process architecture and mechanical design and ensure compliance with cGMP and regulatory standards to enhance design functionality and environmental performance. Click here to learn more.

INDUSTRY INSIGHTS

Quality Metrics: How To Add Value And Meet The FDA's Expectations

Establishing and utilizing quality metrics is essential for the pharma industry's future success. Learn how to identify meaningful metrics and appropriately measure quality to make better business decisions.

A Complete Guide To Capsule Checkweighing

Understand why accurate capsule weighing is essential for therapeutic efficacy, safety, and adherence to pharmaceutical manufacturing standards.

The Business Value Of Connectivity For Product Inspection Equipment

Realize the value of connectivity, and more specifically, the value of the information provided by checkweighing, metal detection, vision inspection, and X-ray inspection.

5 Trends Impacting CMOs In 2025

In 2025, CMOs will navigate Annex 1 compliance, the BioSecure Act’s uncertainty, AI-driven drug development, supply chain challenges from tariffs, and pandemic preparedness strategies.

Barrel Filling Vs. Tip Filling A Syringe – Which Approach Should Be Used?

There are two primary filling methods for pre-filled syringes. Explore the pros and cons of each approach, highlighting why barrel filling is generally preferred in the pharmaceutical industry.

Effective And Consistent Chemical And Microbiological Cleaning

Issues related to cleaning and cleaning validation are some of the most common concerns that arise in FDA Warning Letters. Discover how to ensure you pass your cleaning validation tests.

Fundamentals For Bispecific Antibody-Based Cell Line Development

BsAbs’ dual specificity opens a wide range of applications. Find out why the consistent production of structurally complex molecules that exhibit high yield and purity requires keen expertise and experience.

Improve Scalability And Manufacturability Of A Cytotoxic ADC

Read about the process conditions and protocols that were chosen as optimization targets and the resulting improvements to ADC production and purification that assessing these parameters provided.

The Seamless Path To Market: End-To-End CDMOs As Your Strategic Ally

Partner with an experienced end-to-end CDMO to streamline development, reduce risk, and accelerate your drug’s path to market in today’s complex and competitive pharmaceutical landscape.

Strategies For More Efficient Mixing Operations

The most common cause of downtime is the use of incorrect or out-of-date equipment. Uncover considerations for improving your processes and increasing productivity.

Overcome Biologics Development And QC Challenges

Although biologics are becoming more and more popular, their development and quality control remains extremely challenging. Here, we provide some useful insight to address challenges as early as possible.

Seamless Process Transfer Using An In Silico Bioreactor Scaling Tool

Transferring cell cultures between scales is challenging and error-prone. Examine a bioreactor scaling software that predicts optimal settings to enable efficient scale-up and progression to clinical studies.

Using AI-Analysis And High-Content Screening To Improve Data Capturing

Gain insight into advanced 3D imaging for drug discovery that features high-throughput, high-quality images, modular hardware, and intuitive software for precise, rapid analysis.

FEATURED EDITORIAL

Using Virtual Reality To Enhance Aseptic Contamination Control

Technologies such as virtual reality (VR), augmented reality (AR), or mixed reality can help alleviate some of the long-standing issues in aseptic contamination control. Here's how.

SOLUTIONS

Single-Use mAb Process Playbook

Scientist Spotlight: Kelly McGuill

Advancing Precision And Automation In Injectable Drug Delivery

Cleaning Detergent: Low-Foaming High Alkaline Liquid

A QMS Software That Enhances Operational Excellence

Vaccine API Weighing And Processing Glovebox Workstation

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