Newsletter | February 28, 2026

02.28.26 -- At JP Morgan 2026, Few Showed Up For U.S. Manufacturing

FEATURED EDITORIAL

At JP Morgan 2026, Few Showed Up For U.S. Manufacturing

Leveraging Conventional Therapeutics Skills For Cell And Gene Therapy

From Biology Grad To Manufacturing Guru

Real-World Phase-Appropriate Control Lessons For mAb/ADC Manufacturers

End-To-End ADC Manufacturing Works Best With Active Sponsor Oversight

Process Engineering's Key Role In Sterile Injectable Facility Design

The Top 10 Nations Redrawing The Outsourcing Map

This Industrial Fungus Has Protein Expression Promise For Pharma

The Quiet Case For Trusting CDMO Pricing

What To Know About — And How To Apply For — FDA's PreCheck Pilot

INDUSTRY INSIGHTS

3 Keys To Success When Planning With Your CMO Partner

A Bridge To The Future: Our World-Class Site In Bridgeton

Developability Assessment And Early Formulation Studies

End-To-End Biologics Support

Expert Insights On Outsourcing In A Dynamic Biopharma Landscape

Liposomes — Challenges And Opportunities

Can Your Cleaning And Monitoring Withstand Regulatory Scrutiny?

Why The Latest E2500-25 Standard Revision Demands Immediate Action

Accelerating Drug Development: Flexible And Fast DNA-To-IND Programs

Flow Chemistry For Contemporary Isotope Labeling

Achieve Speed, Stability, And Compliance In Cell Line Development

Optimizing Bispecific Antibody Expression

Accelerating A Complex Molecule From CLD To cGMP In 12 Months

FDA's Regenerative Medicine Advanced Therapy (RMAT) Program

CDMO Trends Impacting 2026

Intelligent mRNA Manufacturing Through Process Analytical Technologies

From Promise To Patients: Pathways To Scale In CGT Manufacturing

Advancing Scalable Vector Production For AAV-Based Treatments

Managing Cell Therapy Investigational New Drug (IND) Timeline Risks

Leveraging Technology For Rapid Clinical Material Delivery

Balancing Early-Stage Needs With Future Success

Enhancing AAV6 Vector Production For Cell Therapies

Mastering Ophthalmic Drug Formulation And Testing

A Smarter Way To Elevate Micronization Output

An Equitable Way To Meet On-Site Business Needs

Redefining OSD Development Through Foresight And Innovation

Cleaner Chemistry For Faster, Higher‑Quality Peptide Production

The Principles Of Green Chemistry: Design For Energy Efficiency

Tailoring Formulations To Meet Precision‑Medicine Needs

Bioequivalence In Topical Generics: Regulatory Considerations

Advanced, Tailored ADC Solutions

Efficient Development Of Biologics

mRNA Vaccines And Therapeutics: Current Trends And Perspectives

Benefits Of Outsourcing To An Integrated CDMO

Pharma Outsourcing Goes Green

Periodic Counter Current Chromatography: A Step Toward Continuous DSP

CDMOs - Key Collaborators In Streamlining Drug Development

Building Bioanalysis Infrastructure For Modern Drug Development

Streamline Biopharmaceutical Manufacturing With Versatile Platforms

3 Keys To Drug Discovery Success — Foresight, Hindsight, And Insight

N-1 Perfusion Strategies For Commercial-Ready Biologics

Global Reach, Biotech Speed: Clinical Packaging, Labeling That Delivers

FIH: Reach Milestones Sooner With A Technology-Driven Approach

Optimizing CMO Partnerships

De-Risking FIH: Integrated Strategies For Rapid Proof-Of-Concept

Overcoming Manufacturing Challenges For Accelerated Drug Development

Mastering Modern Challenges Through Expert Technology Transfer

What Biotechs Should Look For In A CDMO Partner Pre-Commercialization

Layer By Layer: 3D Screen Printing And The Future Of Drug Development

How To Approach Brazil's Regulatory Compliance

Reducing Wastewater Incineration And Carbon Emissions

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