Newsletter | February 26, 2026

02.26.26 -- Facility Considerations When Retrofitting Legacy Sites For ADCs

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Adventitious Agent Testing by NGS: A Comprehensive Solution with Targeted and Non-Targeted Methods

Regulatory agencies expect extensive screening of cell banks for both endogenous and adventitious viral contaminants. The testing strategy should be risk-based and consider key factors such as the origin of the cell line, including the species from which it was derived, and the history of the cell bank itself. Read this white paper to explore a comprehensive adventitious agent testing strategy!

FOCUS ON FACILITIES DESIGN & MAINTENANCE

Facility Considerations When Retrofitting Legacy Sites For ADCs

Antibody-drug conjugate manufacturing requires, among other things, unidirectional flow and air locks for people and materials. Facilities often lack these attributes.

Sustainable Freezing In Biopharma

How does this pivot to natural gas-driven refrigeration platforms in the pharmaceutical manufacturing arena pose challenges and is sustainable cryopreservation possible?

Connection Technologies Enable Modular Single-Use Systems

Single-use systems are increasingly prevalent in biotechnology processes. Explore the benefits, challenges, and solutions presented by modular single-use systems.

Sourcing Pharmaceutical And Industrial Equipment In Auctions

More and more industrial gear is hitting the auction block. Unlock significant savings by understanding the nuances of pharmaceutical and industrial equipment auctions.

Selecting The Right Single-Use Materials In Biopharmaceutical Manufacturing

Manufacturing operations are getting a boost thanks to single-use technologies, but how do biopharmaceutical manufacturers choose the right materials for constructing their single-use solutions?

What's The Real Challenge In Biologic Manufacturing Scale-Up?

As you plan your next stage of scale-up, take a moment to evaluate whether your manufacturing strategy is built around capacity — or around evolving market demand.

FOCUS ON FACILITIES DESIGN & MAINTENANCE SOLUTIONS

A Single Resource For Total Cleanroom Confidence - AES Cleanroom Technology

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Where Biologic Stability Programs Fail—and How ICH Q1 Can Help You Get It Right

Stability is no longer a back-end regulatory checkbox. In this Catalent webinar, experts unpack how the draft ICH Q1 guidance moves stability to the front lines of biologics development and risk management. Learn what’s changed, why legacy approaches fall short, and how to redesign stability programs using case studies to uncover hidden risk early. Click here to learn more.

FOCUS ON MANUFACTURING CONTROLS

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.

Predicting The Performance Of Perfusion Media In A Continuous Bioreactor

Small-scale perfusion-mimic models can effectively predict media performance in continuous bioreactors to help optimize cell density, productivity, and scalability for CHO cell lines.

The Impact Of Artificial Intelligence On CQV

AI is revolutionizing CQV in life sciences by automating documentation, enabling real-time monitoring, and driving predictive quality to boost efficiency and compliance across validation processes.

Accelerating Manufacturing Digitalization With Low-Code Development

Learn how a low-code approach to MES systems delivers speed, flexibility, and compliance, empowering manufacturers to overcome bottlenecks and embrace digital transformation with confidence.

Leveraging Life Sciences Data For Intelligent Decision-Making

Industry 4.0 drives life sciences to prioritize data-driven decision-making by integrating advanced technologies in QMS. Discover how modern data management can improve compliance.

How GMP And Clinical Rules Shape Upstream Discovery And Development

Early collaboration between R&D and manufacturing ensures regulatory readiness and efficiency. See how automation and robust panel design enable clinical translation for advanced development.

Moving Batch Release Into The Fast Lane

Complex supply chains and fragmented systems slow batch release, delaying patient access. Find out how automation and centralized data improve compliance and accelerate delivery.

MANUFACTURING CONTROLS SOLUTIONS

Managing Complex Data In Process Development And CMC - Danaher Life Sciences

A Powerful Platform To Speed Up Operational Efficiency And Time-To-Market - Honeywell Life Sciences

Nanopositioning System Built For Compatibility - Mad City Labs, Inc.

Evolve From Paper To Digital Operations Quickly And Simply - Aizon

Accelerate Workflows With An Adaptive Closure - Nordson MEDICAL

Top 10 Reasons To Move From On-Premise Systems - IDBS UK HQ

Integration That Powers Real-Time Automation Across Your Enterprise - Blue Mountain

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