Newsletter | December 14, 2025

12.14.25 -- Shaping The Future Of GLP-1 Quality

FROM THE EDITOR

Shaping The Future Of GLP-1 Quality

Three experts—Doug Bakan (CTO of Kailera), Hyung Heon Kim (CEO of MetaVia) and Deepa Nagpal (Founder of SygnifyQ)—joined us on Oct. 15, 2025, to explore this topic, find out the most common quality failures, learn what innovation is occurring and find out what business decisions can help support both quality and quantity.

Innovation, Growth (And Happiness) Projected For Pharma

Leaders In The Excipient Market: Region And Type

INDUSTRY INSIGHTS

What Does The New Annex 1 Mean For The Aseptic Fill/Finish Industry?

6 Reasons To Consider HVLD Vs. Vacuum Decay For Pharma Products

Friendshoring: A Strategic Shift In Pharma Supply Chains

Leak Rate Testing for Freeze Dryers: A Scientific Approach

Advancing Multiomics Through Intelligent Automation

The Impact Of AI In Biopharmaceutical Manufacturing

Low Temperature Storage Containment For Vial And Syringe Systems

A High-Throughput Platform For Fast And Reliable Clone Screening

Improving Uptime In Aseptic Processing Of Pharmaceutical Liquids

Continuous Flow Chemistry (Processing) For Intermediates And APIs

Adapting Single-Use Chromatography To Manufacturing Scale

How To Shift From Animal-Based Pyrogen Testing To In Vitro Testing

The High Requirements Placed On Pharmaceutical Labeling Solutions

Considerations For Buffer Preparation As You Grow

New Approaches To Tailored Release Profiles

Reducing Wastewater Incineration And Carbon Emissions

Optimizing Contamination Control: Strategy Planning And Execution

Formulation Technologies For Developing Dry Powders For Inhalation

The Challenges Batch And Continuous Manufacturing Bring To Containment

Navigating Digital Transformation For Pharmaceutical CDMOs

Why Manual QbD Leads To Delays, Errors, And Ongoing Frustrations

A Driving Force For Advanced Cleanroom Standards

De-Risking FDA Abbreviated New Drug Application (ANDA) Submissions

Patient-Centric Solutions To Optimize Medication Adherence

Breaking Down The Barriers To Digitalization In Pharma Manufacturing

Collaboration For Clinical To Commercial Manufacturing Success

How To Drive Digital Manufacturing In Regulated Industries

The Commercial Advantage Of Softgels

Integration Of Container Closure Integrity In Contract Manufacturing

Meet Regulation Requirements With RTU Vials And Cartridges

Strategies For More Efficient Mixing Operations

Enhancing Process Lifecycle Management For Optimized Drug Development

Investing In Capacity – API Commercial Manufacturing

Helping Deliver At Lightspeed With IMEx

The Fourth Industrial Revolution: Robotics And The Laboratory

The 3 Cs You Should Expect From Your Pharma Service Provider

The Hidden Threat To Product Purity: Neglected Seals In Synthesis Columns

10 Steps To Digital Validation Budget Success

Spray Drying For Improved Solubility

Winning Strategies For Oral Dosage Form Development And Manufacturing

Growing A Sustainability Culture Across An Expanding CDMO Network

Multiple Fill Line Delivery Experience

The Role Of Micronization With Dry Powder Inhaler Technologies

Achieve Pharma 4.0 With Next Generation Software-Defined Manufacturing

Characteristics Of Environmental Residues And Protocols For Removal

Ensure Speed And Success With Your Drug Delivery Project

Optimizing TFF And SPTFF For High-Concentration mAb Formulations

Environmental Monitoring Handbook For Pharmaceutical Manufacturers

How To Optimize CMC And Clinical Strategies For Peptide Drugs

Studying Analyte Binding To Syringe Filters During Filter Validation

Guide To Product Inspection Systems In The Pharmaceutical Industry

Choosing Sterile CMOs: Aligning cGMP Standards With Product Needs

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