11.13.26 -- Modulus Brings Home Top Award At 2026 FOYAs

Fragmented automation slows data and strips the context. Manufacturers are moving toward connected plants, where integrating control, execution, and knowledge systems is becoming the expectation.

Explore the key advantages of stick-pack formats for pharmaceuticals and nutraceuticals, from enhanced product safety and cost-efficiency to improved compliance and marketability.

Radiofrequency identification (RFID)-based unit-level tracking solutions for prefilled syringes are poised to help pharma manufacturers address key risks and costly bottlenecks related to the fill-finish process.

Improve medication adherence and health outcomes by developing patient-friendly dosage forms that enhance swallowability and palatability for pediatric, geriatric, and dysphagic populations.

See how endotoxin assays use Factor C activation to generate measurable absorbance or fluorescence signals, with guidance on selecting detection formats and implementing scalable workflows.

Devoting early-phase resources for solid form understanding and screening during a drug’s development lifecycle is critical, as doing so can help save time and resources on the path to market.

Understanding formation mechanisms and potency categorization allows developers to mitigate risks early, ensuring regulatory compliance and patient safety without compromising product performance.

Switching on an audit trail shows awareness, not control. Inspectors look for governed review: defined scope, structured reasons for change, risk-based cadence, and more in maintenance and calibration.

Enhance containment and process reliability in oral GLP-1 synthesis. Discover how integrated single-use assemblies and automated fluidics safeguard chemical purity during scale-up.

Potency bands and exposure limits are a starting point, not the answer. Quantity, dustiness, transfer method, and process energy determine whether a control fits weighing and dispensing.

Hidden gaps in process maturity and organizational alignment can derail development. Discover how to identify risks early and improve readiness for key milestones.

Uncover the rising challenges of recall management in life sciences. This six-part series offers expert insights and unveils a groundbreaking solution set to transform how companies manage recalls.

Delve into practical ways to improve stickpack production through accurate dosing, reliable sealing, automated quality control, and efficient material handling while reducing complexity.

With FDA no longer identifying Q1/Q2 differences, applicants bear the diagnostic burden. Reverse engineering now directly affects development speed, cost, and approval.

Find out how innovative and safer synthetic strategies can streamline the manufacture of Upadacitinib while addressing the complexity and safety challenges inherent in its key intermediates.

Climate targets are only the beginning. Real progress depends on operational efficiency, supply chain collaboration, and accountability.

Discover how AI converts traditional environmental monitoring into predictive intelligence that prevents contamination events before they occur, fundamentally changing cleanroom quality control.

Integrating regulatory strategy with R&D planning early in drug development helps to minimize formulation risks and align manufacturing with compliance while preventing costly delays.

A fully integrated single‑site model unifies development, manufacturing, formulation, fill‑finish, and quality oversight to reduce handoff risk and speed progression from API to sterile drug product.

Modern drug manufacturing requires a shift toward partnerships that prioritize agility and quality. Success depends on specialized expertise and technical collaboration to navigate requirements.

Structured ESG frameworks drive resource optimization, waste reduction, and workplace safety across production lifecycle phases. Examine actionable insights for responsible manufacturing strategies.

Sterile manufacturing requires built‑in contamination control, using strong utilities, purified water, clean steam, controlled gases, pressure management, and qualified single‑use systems.