Newsletter | June 13, 2025

06.13.25 -- Early-Phase Formulation Done Right: An Expert Analysis

SPONSOR

20-minute capacity and capabilities quick-looks, 20+ brand new CDMO presenters to evaluate for best-fit this quarter – and a (virtual) commitment of less than 20 percent of your day? We’re confident you don’t need 20/20 vision to see the value in this! Join us for Outsourced Pharma’s July Partner Week – including sessions in Small Molecule API/HPAPI, Small Molecule Finished Dosage Form, ADC, Analytical Services, and Fill/Finish among others. Registration, on-demand access, and interactive Q&A are free.

INDUSTRY INSIGHTS

5 Must-Haves In A Contract Packaging Partner

A partner should function as an extension of the pharma’s organization, so careful consideration should be devoted to initiating this relationship. 

From Pegylated Shells To Glucose-Responsive Acts

Explore our full collection of case studies to discover how liposome technology is transforming drug delivery across a wide range of therapies.

Customized Release Through Dispersed Dosage Formats

Typically, dosage format is based on the target product profile: how the developer envisions the product best addressing a clinical indication by maintaining population-wide efficacy.

FEATURED EDITORIAL

Early-Phase Formulation Done Right: An Expert Analysis

Dileep Boinipally has extensive experience in formulation, manufacturing process development, and regulatory strategy. He’s adept at explaining all that, but Chief Editor Louis Garguilo got him to focus for readers on the ins-and-outs of the practice of early formulation development.

Should Your CDMO Run 'Technical' Batches?

Our panel pitches in on the need for "extra" technical, tox or engineering batches to further ensure manufacturing success, and considering tight budgets at biotechs.

INDUSTRY INSIGHTS CONTINUED

'Ultra High' Potency Development And Manufacture

A biotech with limited experience in the development of high-potency compounds sought to develop a process for producing a highly potent API used to treat an unmet oncology need.

Right-Sized For Success: The Benefits Of A Boutique CDMO

Partner with a right-sized CDMO to gain the agility, expertise, and personalized focus needed to accelerate your drug development with confidence.

Improve The Performance Of Your Small And Large Molecule Medicines

Examine the latest in nanotechnology advancements, including recent clinical data, formulation applications, and API optimization to NanoImprove formulations.

Solutions For Accelerated Pharmaceutical Development

Discover an integrated service package designed to simplify and accelerate the development pathway, even for APIs with challenging properties such as low aqueous solubility and poor bioavailability.

SPONSOR

The PDA Regulatory Conference 2025 Achieving CGMP Excellence: Sustainable Compliance Across the Lifecycle continues its 34-year tradition of delivering impactful content that supports the development and implementation of effective quality systems across the product lifecycle. This premier pharmaceutical CGMP conference on 08-10 September 2025 in Washington, DC will focus on strategies to manage manufacturing and quality risks while driving operational excellence and sustainable compliance.

SOLUTIONS

Capacity Update October 2024: Small Molecule

Learn how recent investments have expanded the capacity for developing, manufacturing, and packaging highly potent drug products.

Predictive Modeling Services

Early identification of potential absorption risks is critical for rapid and efficient drug development. PBPK modeling services are designed to de-risk your drug development program.

Bridging Molecules From Early Discovery To POC And Beyond

This partnership improves flexibility for customers, offers dedicated project teams, and enables a bespoke service that is tailored to each development program.

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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