Newsletter | February 26, 2025

02.26.25 -- No Shadow Organizations Needed (Stick To Your Virtual Model)

FEATURED EDITORIAL

No Shadow Organizations Needed (Stick To Your Virtual Model)

Co-founder, President, and CEO of EQUULUS Therapeutics Robert Discordia knows that to advance early-stage development assets most economically, biotechs should: (a) stay within their virtual model, and (b) base that outsourcing strategy on initial business objectives. Here are his dos and don'ts.

Growth And Trends In Topical Drug Contract Manufacturing

Rising incidences of dermatological conditions, including acne, psoriasis, and skin cancer, are driving growth in topical drugs. Pharma companies are increasingly using contract manufacturers.

INDUSTRY INSIGHTS

Tablet Edge Erosion – Solutions For Friability

Addressing tablet edge erosion and friability involves adjusting formulation, tablet design, tooling, press setup, and operation speed to improve tablet robustness and reduce weight loss.

A Proven Approach To Impurity Control Across API And RSM Synthesis

To help manage impurities and mitigate risk across all stages of development, consider the benefits of working with a CDMO that has robust chemistry understanding and manufacturing experience.

Expanding The OSD Toolbox: How To Adsorb Lipids Onto Powder Substrates

Explore innovative solutions for improving the solubility and bioavailability of poorly soluble compounds in solid oral dosage forms to enhance drug delivery and therapeutic effectiveness.

Simultaneous Spray Drying For Large/Small Mol Combinations

Gain insights into a “simul-spray” process pioneering for combining small and large molecules into a single, atomized drug product for inhalation administration.

Innovative ASD Technology Improves Abandoned Cancer Medication

Here, we look at how one solid dispersion technology lowered patients' pill burdens and demonstrated an improved therapeutic response for Galeterone.

SOLUTIONS

Choosing A CDMO For Oral Solids, Nasal And Pulmonary Dosage Forms

Consider the many advantages of partnering with a CDMO, including their extensive expertise and capabilities across oral solids and specialized nasal and pulmonary formulations.

Nasal Spray Development And Manufacturing Services

A partner with experts who are adept at working with complex, sensitive, and potent APIs, screening for the optimal formulation, and scaling up efficiently is vital for successful trials and commercialization.

Regulatory Starting Materials (RSMs) — India

Our innovative business model doesn't add additional costs to your project. Review our network's regulatory starting material capabilities and contact us to simplify your solutions.

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.

Connect With Outsourced Pharma: