03.08.26 -- The Rise Of The Autonomous Pharma Plant

FROM THE EDITOR

FEATURED EDITORIAL

MES Is Still In The CD ROM Era But The Data Architecture Has Moved On

By Ciera Clayton, BioPhorum

Rethinking Product Development Through Lipid-Based Formulations

By Eduardo Jule, Ph.D., Evolve Consulting

INDUSTRY INSIGHTS

Advance Long-Term Cell Kinetics With Integrated Fluid Handling

Tecan

Winning Strategies For Oral Dosage Form Development And Manufacturing

By Dave Miller, AustinPx

Dynamic Precision Weighing Challenges And Innovations

Mettler-Toledo Product Inspection

High-Content Imaging Drives Protein Degraders From Hit To Lead

By Clark Driscoll, Erin Olin, Adam McCabe, et al., Curia

New Vs. Used Processing Equipment: A Cost Comparison

Federal Equipment Company

Process Re-Design For Sustainability In Small Molecule Manufacturing

Lonza

A Closer Look At Inspection Systems In Tablet And Capsule Production

Anritsu - Product Inspection & Detection

5 Critical PUPSIT Considerations For Sponsors Targeting The EU Market

By Steve Taliadouros, PCI Pharma Services

Effective Environmental Monitoring And Control In Pharma Operations

By Diane Lockard and Alexis Mathews, Eurofins

Inline Buffer Formulation: A Facility Operations Game Changer

By George Flores, Asahi Kasei Bioprocess

Fast-Track Innovation, Address CMC Challenges In Expedited Pathways

Quotient Sciences

Driving Robust Tech Transfer In Biologics: Computational Fluid Dynamics

Samsung Biologics

Why Compounding Pharma Manufacturers Should Evaluate BFS Systems

By Andy Goll, Weiler Engineering, Inc.

Demonstrating Value Throughout The Product Development Life Cycle

SGS

Enhancing Automated Environmental Monitoring In Gloveless Isolators

MilliporeSigma

Remote Measurements For Bulk Samples

By Matthew Gabel, Ph.D., Thermo Scientific Product Inspection

Right From The Start: Smarter Developability For Stronger Formulations

By Nazar Elkarim, Ph.D., Mikart

Rapid, Material-Sparing Feasibility Screening For Hot Melt Extrusion

Lonza

Strengthen Pharmaceutical Supply Chains With A U.S.-Based CDMO

Grace Fine Chemical Manufacturing Services

Monitoring, Media Fills, And QC: Demonstrating Sterility Assurance

Afton Scientific

Optimizing Virus Filtration Validation

By Aernout Martens, Cytiva

Enabling CDMOs To Focus On Core Priorities

Thermo Fisher Scientific

Design–Build Cleanroom Projects: A Proven Risk Mitigating Methodology

By Matt Dean and Mitchell Gonzales, AES Cleanroom Technology

The High Requirements Placed On Pharmaceutical Labeling Solutions

HERMA

How T3P Can Enable Greener, Cost-Effective Peptide Synthesis

Curia

Sustainable Solutions For Medical Devices

dsm-firmenich

Meet Regulation Requirements With RTU Vials And Cartridges

By Giovanni Cosmi, Mirko Gabriele, and Andrea Salmaso, Stevanato Group

Quality Management Fundamentals For Modern Compliance

By Jak Kane, Ideagen

Robotics And Automation Addressing Production Shortages

AST

Validation Provider Shortens The Path To Equipment Qualification

ValGenesis

Friendshoring: A Strategic Shift In Pharma Supply Chains

Bora Pharmaceuticals

How Digital Procedures And E-Logbooks Are Transforming Manufacturing

Honeywell Life Sciences

Harnessing Chemistry For Scalable Manufacture Of Lipids Used In mRNA

Curia

Inside The Shift Toward Greener, Faster, Smarter Drug Manufacturing

By Dave Henderson, Ph.D., Asymchem

Reflecting On 2025: Innovation And Investment

ROIS

Navigating Bioconjugate Development

Lonza

Advancing Drug Safety And Improving R&D Productivity

Emulate

Solving Delivery Challenges For Tolerogenic Vaccines

Catalent

Powering Pharma: Digital Innovation And Sustainable Solutions

Ecolab Life Sciences