Newsletter | May 7, 2026

05.07.26 -- Using PATs For Real-Time Process Monitoring

SPONSOR

At AAPS, drug product experts discuss how formulation, stability, and analytical services enable robust CMC strategies, reduce development risk, and support confident regulatory decision making. Learn more

FOCUS ON MANUFACTURING CONTROLS

Using PATs For Real-Time Process Monitoring

In this segment from the Bioprocess Online Live event, “Aligning CMC And MSAT To Move PATs Out Of Pilot Mode,” our panelists respond to results from an audience poll. Audience members indicated they use PATs for real-time process monitoring more in upstream than in downstream. 

The Business Case For Continuous Manufacturing In Biologics

The question for leadership is not if continuous manufacturing will transform biologics, but when and how quickly to invest.

Digital Solutions Enhance Pharmaceutical Manufacturing Performance

Personalized therapies and advanced technologies are reshaping manufacturing. Explore how intelligent automation can improve flexibility, strengthen data integrity, and accelerate production.

How A New Partnership Is Making Compliance Easier For Life Sciences Teams

When compliance gaps disrupt equipment programs, the consequences show up fast. Learn how pairing digital systems with practical expertise helps teams standardize processes and stay inspection-ready.

Richter BioLogics Drives Efficiency And Compliance With Unified Quality

See how one CDMO tripled production, improved audit readiness, and built customer trust by unifying quality systems and embracing a digital-first approach.

The Key To Optimizing Operational Value

Watch to discover transformative opportunities in the life sciences industry as well as how to unify digital quality and manufacturing processes to stay ahead in this dynamic field.

Innovation And Efficiency - Visual Inspection In The 21st Century

Digitizing your visual inspection processes is key to unlocking efficiency and ensuring compliance with global regulatory standards. Find out how to transition from paper-based systems to a digital database.

How Many Of These 7 ADC Handling Considerations Do Have On Your Radar?

Your ADC handling protocol may have gaps you have not accounted for yet. Examine seven considerations that are reshaping how manufacturers protect product integrity and operator safety.

Cloud Migration In Regulated Environments: Validation And Best Practices

Cloud adoption is essential for BioPharma growth, offering scalable tools for faster research. Success requires a risk-based approach to ensure data integrity and GxP compliance during the shift.

Future-Ready Process Control: Enabling AI And Digital Transformation

Failing to innovate limits your agility and adaptability. When implemented thoughtfully, AI and automation can improve integration, efficiency, and compliance without compromising integrity.

Overcoming The Data Hurdle: Defining 'Good Data' For Agentic AI

Agentic AI delivers real value only when supported by contextualized data. Gain insight into how unified data fabrics transform siloed records into actionable intelligence, enabling faster decisions.

How Integrated Data Systems Enhance Clinical Development

Delve into how cloud-based systems and unified data platforms are transforming biomanufacturing by enhancing efficiency, ensuring quality, and accelerating the delivery of complex therapies to market.

MANUFACTURING CONTROLS SOLUTIONS

Microscope For Fluorescence Microscopy - Mad City Labs, Inc.

End-To-End Digital Validation - CAI

A Fast And Simple ddPCR Assay For In-Depth AAV Characterization - Bio-Rad Laboratories, Inc.

Multimode Plate Reader With Live-Cell Imaging And Real-Time Cytometry - Tecan

Production Lifecycle, Bioprocess R&D, Scale-Up, Tech Transfer, Validation, And Mfg - Koerber Pharma

SPONSOR

Webinar: Design scalable downstream processes with practical purification and analytical strategies

Explore how to build robust, scalable downstream purification processes across today's complex modalities. In this Cytiva webinar, experts share practical chromatography strategies, advanced analytical insights using SPR and SEC-MALS, and real-world case examples to help reduce risk, solve impurity challenges, accelerate development, and strengthen long-term internal process knowledge and operational efficiency from proof of concept through scale-up. Click here to learn more.

FOCUS ON FACILITIES DESIGN

The Case For A Facility Monitoring System

Facility monitoring software with OPC UA client/server functionality makes great business sense. Uncover how monitoring leads to reduced waste, improved yield, higher quality, and increased profits.

MTP And "The Ballroom Concept": Agile Manufacturing For Pharma

Modular automation is reshaping manufacturing by enabling faster changeovers, reduced downtime, and built‑in compliance. Understand how the “ballroom” approach helps teams adapt to shifting demand.

How To Inspect Used Stainless Steel Tanks And Reactors To Avoid Risk

Used stainless steel tanks can cut costs and lead times, but only with a thorough evaluation. Verify specifications, inspect welds and surfaces, and confirm dimensions to ensure reliable performance.

Determining The Power Numbers For A Single-Use Mixing System

In designing a mixing process for scale-up, the power number is a critical parameter. Explore the determined power numbers for a single-use mixer at various mixing speeds and fill levels.

FACILITIES DESIGN SOLUTIONS

Versatile Tube Welding - Ensorcell

Connect With Bioprocess Online: