Newsletter | October 1, 2025

10.01.25 -- N=1: Redefining Clinical Pathways For Ultra-Rare Disease Treatment

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Explore 20+ new CDMO presenters in quick 20-minute sessions during Outsourced Pharma’s October Partner Week (Oct. 6-10). Sessions include Analytical Services, ADC, Large and Small Molecules, Cell and Gene Therapy, and Fill/Finish. Each session offers a quick, informative look at capabilities to help you find the best-fit partner. Registration, on-demand access, and interactive Q&A are all free. Save your spot today!

FEATURED ARTICLE

N=1: Redefining Clinical Pathways for Ultra-Rare Disease Treatment

The N=1 frontier isn't just about helping the rarest patients, it's about building the infrastructure for medicine's future, write experts at Uncommon Cures.

INDUSTRY INSIGHTS

Five Questions Biotechs Should Ask Before Selecting A Bioanalytical CRO

In a landscape where speed, quality, and trust are inseparable, choosing a CRO that shares your ambition is not optional; it is essential to survival and success.

A Fair, Ethical Framework For Participant Payments In Clinical Trials

Participant payments in clinical trials have long been fraught with inconsistency, raising questions about the role of IRBs, tax implications, and fair reimbursement structures.

The Forgotten Stakeholder: Why Caregivers Are The Key To Clinical Trial Success

By designing protocols and support ecosystems that address caregiver concerns, sponsors not only improve trial outcomes but also foster trust and advocacy within family-dependent populations.

6 Steps To Help You Choose The Right Clinical Trial Partner

The right digital partner can unlock speed, scale, and collaboration that can transform the future of your pipeline. Uncover the six steps to help you choose the right partner for your trials.

Optimized Expression Systems For Increased Productivity

Discover innovative strategies to boost CHO DG44 cell line productivity, as well as explore optimized expression systems that enhance yield, stability, and efficiency in protein development.

Project Orbis Drug Registration 2025

Project Orbis helps streamline the review and approval of oncology medicinal products through international regulatory collaboration. Learn how this framework can accelerate your regulatory strategy.