Newsletter | January 16, 2026

01.16.26 -- You're In Charge Of Strategic Sourcing? What's That Actually Mean?

INDUSTRY INSIGHTS

Effective Environmental Monitoring And Control In Pharma Operations

A structured contamination control strategy uses the Plan, Do, Study, Act model, focusing on EMPQ, meticulous planning, trend analysis, and continuous improvement with CAPA and change control.

Our Approach To Regulatory Compliance In China

Leverage proven regulatory expertise and local support to turn China’s rigorous API requirements into a clear, efficient pathway to market success.

Best Practices For Regulatory Excellence In Clinical Research

Observe how GCLP can integrate ethical and technical standards to ensure reliable, compliant clinical trial data and optimize laboratory operations across sponsors, CROs, and partners.

FEATURED EDITORIAL

You're In Charge Of Strategic Sourcing? What's That Actually Mean?

Chief Editor Louis Garguilo wraps up his investigation into the real meaning of "strategic" when it comes to supply chains, sourcing, procurement, and outsourcing development and manufacturing to CDMOs. He discovers a series of best practices that turn one-off tactics and isolated decisions into multi-variable and thoughtfully aligned relationships.

Establishing Realistic Development Timelines With A CDMO

This segment of the Outsourced Pharma Live event, “Small Molecule Outsourcing: Getting Timelines, Tech Transfer and Analytics Right," details how sponsors can build realistic development and manufacturing timelines with CDMOs by combining complete transparency, upfront risk assessment, phase-based planning, and shared Gantt-style project dashboards instead of rushing straight from research to GMP, featuring panelist Vadim Klyushnichenko, VP Bio/Pharmaceutical Development & Quality at the Calibr-Skaggs Institute for Innovative Medicines.

INDUSTRY INSIGHTS CONTINUED

How To Capture Growth In The Expanding Metabolic Drug Market

Driven by GLP-1 success and rising obesity rates, R&D investment in metabolic disease therapies now rivals oncology, demanding rapid development to overcome market challenges.

Advanced Analytical Tools To De-Risk Pharmaceutical Development

Discover three tools that facilitate a successful journey from candidate compound to clinical triumph: solid form screening, PBPK modeling, and AI-enabled route scouting.

Increasing Bioavailability With Amorphous Solid Dosage Formulations

See the challenges associated with pH-dependent solubility for oral tyrosine kinase inhibitor drugs and how leveraging ASD formulation can help create more effective, patient-friendly drug products.

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.

SOLUTIONS

From The Floor At CPHI 2025: Takeaways Everyone Should Know

Gain insights into evolving pharma priorities, from supply chain resilience to advanced manufacturing, and why flexibility, scalability, and technical expertise matter in a dynamic global market.

Solve Complex Small Molecule Challenges

We specialize in the custom development and manufacturing of small molecule APIs, intermediates, and RSMs, offering scalable solutions from kilograms to multi-ton quantities.

The Future Of Blister Packaging

Maximize your productivity and efficiency with a solution for inline cartoning, bundling, case packing, and pallet loading that also includes thermo and cold forming options to accommodate packaging needs.

Technology Transfer And Commercial Manufacturing Of Tablets And Capsules

Finding a strategic CDMO partner that will offer solutions for your late phase clinical and commercial needs, mitigate risks, and bolster your supply chain is crucial for meeting project milestones on time.

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.

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