Newsletter | June 19, 2025

06.19.25 -- A Psychedelic Path To CDMO Selection?

SPONSOR

Webinar: Transposase-Enabled CLD: From Transfection to High Titer with Ease

Join KBI Biopharma for a webinar on transposase-enabled cell line development. Built on Selexis® SUREtechnology™ and CHO-M™, this platform delivers high titers, rapid development, and stability for complex biologics. Learn how it accelerates timelines, supports diverse molecule formats, and meets regulatory demands—offering a scalable, efficient alternative to traditional CLD methods. Perfect for teams seeking speed, quality, and flexibility in biotherapeutic development. Click here to learn more.

INDUSTRY INSIGHTS

Bioprocess Operation Modes And Advanced Bioreactor Technologies

Explore innovative cell culture methodologies and bioreactor technologies to optimize productivity, enhance product quality, and drive efficiency in biotechnological applications.

Navigating The 'Now What' After Early-Phase Success

While moving from early- to late-phase clinical trials is a critical milestone to celebrate on the way to commercialization, many face the same daunting question once the confetti settles ― now what?

Characterization Of Spray Dried Biologics

Discover how spray drying can transform the formulation of complex biologics by improving stability, delivery, and functionality, with insights into the critical techniques needed for successful development.

FEATURED EDITORIAL

A Psychedelic Path To CDMO Selection?

"Be prepared. Structured. Work in a systematic fashion towards your CDMO selection." That's a rather non-psychedelic paraphrasing of Anthony Grenier, Reunion Neuroscience, a biotech pursuing the development of novel, synthetic psychedelic molecules. Here's more of his thoughts on CDMO selection.

The Promise And Challenges Of Cell-Free Protein Systems

CFPS use cell lysates or purified enzymes to synthesize proteins. They have emerged as a promising alternative to production with living cells.

INDUSTRY INSIGHTS CONTINUED

Key Financial Considerations For Phase 2 Clinical Injectable Drug Manufacturing

Consider the importance of scalability and flexibility in the choice of an early-stage manufacturing strategy and how that decision impacts financial outcomes for a drug development program.

Choosing A CDMO: 3 Considerations For New Drug Developers

A challenge in drug development is finding a team that can carry a molecule from the research lab to the patient’s bedside. Witness three considerations that build a foundation for partnership.

Driving Operational Excellence Using Machine Learning

Examine how advanced machine learning and data analytics are revolutionizing biopharmaceutical manufacturing and driving operational excellence.

Building A Legacy In Sterile Injectables Through Strong CMO Synergy

Learn how a CMO can deliver significant value to drug developers by fostering successful outsourcing relationships, streamlining the path to market, and supporting demands.

Overcoming Barriers To Protein A Membrane Adoption

Understand how using Protein A membrane and resin interchangeably can streamline bioprocessing for efficient, scalable, high-quality manufacturing from lab to full-scale production.

SPONSOR

ChemOutsourcing 2025 is the leading U.S. conference for small molecule API, peptide, oligonucleotide, and drug development services. Held September 2–5 in Parsippany, NJ, it attracts biotech and pharma buyers seeking CDMO partners. With 100+ global CDMOs, expert panels, and targeted networking, it’s the go-to event for small molecule, peptide, and oligo outsourcing, connecting innovators across the global pharmaceutical supply chain.

SOLUTIONS

Capacity Update April 2025: Large Molecule Development

By leveraging our proprietary non-viral gene insertion technology, we ensure rapid development timelines and high-yield production, making an ideal solution for complex biologics.

Specialized Services In Custom Peptide Synthesis

Custom peptide synthesis services provide numerous options for synthesis platforms, purity levels, and modifications to meet a wide range of research needs.

SUREtechnology Platform

Witness how an advanced CLD platform enables high-yield, stable CHO cell lines while overcoming bottlenecks and supporting verification, characterization, and monoclonality assessment.

CDMO Capacity Update April 2025: Large Molecule Development

Experience a global network of expertise and proven manufacturing capabilities that can help accelerate your clinical and commercial drug substance programs.

OUTSOURCED PHARMA CAPACITY UPDATE

Find Your New CDMO At Outsourced Pharma Capacity Update

CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capacities. See for yourself why this virtual event has become a wildly popular resource to identify options for your development and manufacturing needs.

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