Newsletter | March 12, 2026

03.12.26 -- Six Specialized Modalities Testing CDMO Readiness In 2026

SPONSOR

Avoiding Scale-Up Surprises: Applying AI and Rapid Prototyping to Media and Process Development

As biologics grow complex and timelines tighten, early development decisions around media, process, and scalability can create manufacturability challenges. In this webinar, Thermo Fisher Scientific experts explore how AI insights, data modeling, analytical testing, and rapid prototyping help teams evaluate choices earlier, reduce risk and prepare programs for cGMP scale-up and manufacturing readiness. Click here to learn more.

FOCUS ON OUTSOURCING

Six Specialized Modalities Testing CDMO Readiness In 2026

As biopharma pipelines shift toward more complex therapies, sponsors are finding that CDMO readiness now depends less on general capacity and more on highly specific technical capabilities.

Proactive Approaches To Minimizing Cell Culture Media Variability

Variability reduction programs improve biomanufacturing by controlling raw‑material complexity, optimizing critical attributes, and boosting productivity through data‑driven partnerships.

Setting The Benchmark For Quality In Cell And Gene Therapy Logistics

Compliance with ISO 21973 protocols safeguards the global transport of sensitive therapeutics. Proper supply chain oversight remains the cornerstone for maintaining product integrity.

A Continuous Electroporation System For Viral Gene Therapy

Gain insight into the specialized engineering behind chemical-free, continuous platforms. These scalable systems streamline production workflows while eliminating hazardous reagents.

Scaling AAV Programs From Initial Research To GMP Manufacturing

Achieve faster AAV gene therapy progress by adopting a unified platform for manufacturing. Accelerate your program to GMP readiness with up to 9x higher titers and robust, high-quality full capsid yields.

Navigate Strategic Shifts In Modern Viral Vector Production

Addressing the complexities of viral vector manufacturing through strategic internalization, advanced technologies, and regulatory excellence is crucial for the future of gene therapies.

Trends Shaping The Future Of Cell And Gene Therapy Manufacturing

Discover how automation and digitalization are transforming cell and gene therapy with scalable, decentralized manufacturing and smarter market navigation.

Manufacturing Strategies To Industrialize Autologous Therapies

Implement structured manufacturing workflows to lower expenditures. By refining process reliability, companies can expedite delivery of life-altering treatments to patients in need.

Establishing A Versatile Platform For Intensified Lentiviral Vector Manufacturing

Leverage advanced, space-efficient manufacturing to enhance vector yields. This methodology provides a cost-effective path to scaling production without sacrificing product quality.

SPONSOR

OPT Congress 2026 convenes the leaders advancing oligonucleotide, mRNA, and peptide therapeutics from discovery through commercialization. Across four focused conferences, explore 60+ presentations covering AI-enabled design, next-generation delivery, scalable manufacturing, and emerging conjugate platforms. Join a high-level community driving real translational impact. Use code OPS26ARNA for $200 off registration

Download the brochure to view the full agenda and secure your place March 18–19 in Boston or virtually.

OUTSOURCING SOLUTIONS

Viral Vector Development And Manufacturing Services - Thermo Fisher Scientific

Biologics Discovery Service: From Target To Preclinical Candidates - ProBio

Gene Therapy Services For Viral Vector Manufacturing - SK pharmteco

Rebrand And Renewed Promise For Your Research - LICORbio

Connect With Cell & Gene: