Newsletter | June 26, 2026

06.26.26 -- Causal Mechanism And Effect Analysis: FMEA's Simpler, Effective Alternative

INDUSTRY INSIGHTS

Email Etiquette That Actually Saves Time For Pharma & Biotech

Less inbox fatigue, more productive weeks. Here are simple email habits designed for pharma and biotech teams.

Tailoring Formulations To Meet Precision‑Medicine Needs

Precision‑medicine formulation requires a thoughtful approach to improve performance, support patient needs, and help therapies advance successfully.

Clinical Innovation Meets Manufacturing Excellence

Discover how our ClinDMO model transforms early drug development with on-demand manufacturing, adaptive formulation, and real-time decision-making to accelerate timelines and optimize API use.

FEATURED EDITORIAL

Remember Why You Are Outsourcing

Just over a year ago, AstraZeneca went all in on creating a cell-therapy franchise; Samir Panjwani joined as a supplier-relationship manager. “I’ve been a builder throughout my career,” he says. The question he’s always kept in mind: Why are we in this industry? He discusses his new role, and his “bilateral experiences” supporting manufacturing outsourcing supply chains.

Causal Mechanism And Effect Analysis: FMEA's Simpler, Effective Alternative

This article describes causal mechanism and effect analysis (CMEA) as an alternative to failure mode and effect analysis (FMEA) for analyzing and managing the industry’s risks.

INDUSTRY INSIGHTS CONTINUED

Science To Success: CMC Strategies That Drive Market Readiness

Learn how a scientifically grounded framework for early-phase CMC development, integrating QbD and risk management, de-risks drug development and accelerates the journey from molecule to market.

The Future Of Sustainable Amorphous Dispersion Development

Sustainable amorphous dispersion cuts cost, risk, and timelines by removing solvent waste, simplifying manufacturing, strengthening supply chains, and scaling efficiently to commercialization.

Patented Process For Intermediates Useful For Deucravacitinib

Discover how this patented synthetic approach to Deucravacitinib intermediates can improve yield, simplify purification, and support scalable, regulatory-aligned manufacturing.

SOLUTIONS

Multiparticulates For Modified Release Systems

Drug Product Manufacturing

Maximize Uptime And Yield With This Feeder Base Leveling System

Solid Form Services

OUTSOURCED PHARMA CAPABILITIES UPDATE

Find Your New CDMO At Outsourced Pharma Capabilities Update

CDMOs in biologics, cell and gene, and small molecule share their capabilities and available capabilities. 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: