Newsletter | June 6, 2025

06.06.25 -- A Psychedelic Path To CDMO Selection?

SPONSOR

Webinar: Navigating the new USP Chapter <382> for Elastomeric Closures

Join this webinar to explore USP <382>, effective December 1, 2025, covering required testing for elastomeric closures in parenteral drugs. Learn about compliance, instrumentation needs, and testing strategies, with expert guidance from Alcami. Click here to learn more.

INDUSTRY INSIGHTS

Optimizing Tablets For Even Splitting: The Pressure Sensitive Bisect Design

The pressure-sensitive bisect design allows accurate tablet splitting by maximizing facet width, optimizing angles, and balancing radius values for durability and user-friendly administration.

The Importance Of Operator Equipment Training

Learn why a strong commitment to operator training is essential to prevent production issues, ensure product quality, and safeguard patient safety.

4 Reasons For The Rise In Blister Packaging

Here are the factors that are driving blister to the forefront of pharmaceutical packaging, and at an even faster rate than its current growth.

FEATURED EDITORIAL

A Psychedelic Path To CDMO Selection?

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

Lilly's Calculated Approach To Upgrade Trade-Offs

If the disruption of implementing and adapting to new technology costs more than its benefits, teams should proceed cautiously.

INDUSTRY INSIGHTS CONTINUED

Enabled Form Selection For Oral Drug Products

Review the role of solid form screening and PBPK modeling to enable accelerated timelines desirable in early-phase drug development. Explore formulation maps for ASDs and key criteria for salt screening.

Increase Spray Drying Throughput For Brick Dust Compounds

Here, we discuss three enabling technologies designed to improve drug solubility in organic solvents for spray drying and define the advantages and risks of each technology.

Integrating Phase-Appropriate Quality Standards

Partnering with an experienced CDMO can provide valuable expertise in defining expectations and requirements, while efficiently managing accelerated product development timelines.

SOLUTIONS

Comprehensive Regulatory Support

Consider our expertise across a wide range of global markets. Our experience in securing regulatory approvals and navigating market challenges positions us as a trusted partner.

Wet Nanomilling And Vial Filling

Nanomilling revolutionizes drug delivery by reducing particle size to enhance solubility, bioavailability, and therapeutic efficacy, addressing the challenges of poorly water-soluble APIs.

Unlocking A Reliable Supply Chain

With end-to-end solutions, proven experience in complex formulations, and a commitment to operational excellence, we help you navigate challenges, mitigate risks, and deliver high-quality therapies efficiently.

SPONSOR

Join Outsourced Pharma Live on June 11th at 2pm ET for a virtual panel discussion on the specific challenges of biologics development that must drive CDMOs to embrace more flexible approaches. Registration is free thanks to the support of Curia.

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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