04.26.26 -- 6 Things You Need to Know from Life Sciences Future SW

FROM THE EDITOR

FEATURED EDITORIAL

Where Contamination Control Really Breaks Down In Practice

By Kyle Winn and Adam Walker, W2 Cleanroom Consulting

How To Implement Post-Approval Changes On A Global Level

By Arundhati Sengupta, Mirum Pharmaceuticals

INDUSTRY INSIGHTS

Sustainability Through Automation, Flow Chemistry, And Biocataysis

Asymchem

Identify And Mitigate Absorption Risks With PBPK Modeling

Lonza

A New Look At Subcutaneous mAb Delivery Using Nanoformed Particles

Nanoform

Development Of Scalable Purification For Biotherapeutic Peptides

Waters Corporation

AI And Digital Maturity In Contract Development And Manufacturing

MasterControl, Inc.

Facilitate Handling Of Bulk Powders With Dry Granulation

MilliporeSigma

The Case For A Facility Monitoring System

By Tim Russell, TSI Incorporated

Automated Precision Powder Filling For Annex 1

Dalton Pharma Services

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

By Josh Russell, AST

Optimizing CMO Partnerships

SMC Ltd.

Overcome Common Pre-Filled Syringe Challenges Through Partnership

Curia

Metal Detectors And X-Ray Inspection Systems: What You Need To Know

Thermo Scientific Product Inspection

Inside The Cleanroom: Training Beyond The Checkbox

Contec, Inc.

Accelerating Antibody-Drug Conjugate (ADC) Development

Mesa Laboratories

Extrusion-Based Scale-Up: Performance Through Process Understanding

Lonza

10 Practical Tips For GMP Cleanroom Contamination Monitoring

Particle Measuring Systems

How To Address Your Solid Dosage Processing Needs

Federal Equipment Company

Guide To Product Inspection Systems In The Pharmaceutical Industry

Anritsu - Product Inspection & Detection

Mitigating Powder Flow And Static Issues Using Mesoporous Silica

Grace Fine Chemical Manufacturing Services

How Can Data Translation Challenges In CRO Partnerships Be Overcome?

By Arielle Mann, Danaher Life Sciences

What Is Aseptic Processing?

Cytiva

Evaluating Viral Clearance Trends In Biologics

By Alex Rodriguez and Eric Coberly, Eurofins

2026 Life Sciences Manufacturing Outlook

Tulip

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

Douglas CDMO

Optimizing DSP Development: Faster Timelines And High-Quality Processes

By Kyunghwa Cho, Samsung Biologics

Optimizing The Path From First-In-Human To Proof-Of-Concept

By Matt Paterson, Quotient Sciences

The M.O. Behind Choosing A CDMO: Three Considerations

Curia

Innovative AI-Driven Solutions To Address The Growing Complexity Of APIs

Lonza

A Globally Adopted Drug Delivery Platform

BD Medical - Pharmaceutical Systems

Benefits Of Isolator Technology In Fill-Finish

By Sabrina Zirkle, Jubilant HollisterStier

Optimizing The Path To First-In-Human Clinical Trials: Design And De-Risk

Lonza

When To Consider Material And Personnel Airlocks For Downflow Booths

Esco Lifesciences

Chromatography In Manufacturing: Purification, Resin, And Qualification

CAI

Key Topics And Trends In Aseptic Filling

Cytiva

OEE And Product Inspection

Mettler-Toledo Product Inspection

Navigating The Complex Landscape Of Monoclonal Antibody Manufacturing

AbbVie

What The Best CDMO Relationships Actually Look Like

By Michael Dunn, Afton Scientific

Cell And Gene Therapies: Insights For Faster Batch Release

Veeva

Realizing The Potential Of The Evolving CDMO Ecosystem

By J.D. Mowery, Bora Pharmaceuticals

Top Safety Considerations In Biopharmaceutical Manufacturing

By Katie Keller, Asahi Kasei Bioprocess

Contamination Control Of Particulate And Shuttle Blow-Fill-Seal Compliance

By Andy Goll, Josh Myers, Laura Weidner, et al., Weiler Engineering, Inc.

FAQ: Fermentation And Biocatalysis In Modern Manufacturing

Curia