ISPE believes moving to Pharma 4.0 represents a competitive advantage to the extent that not embracing its potential might be a business risk for pharma companies.
Today’s developing environment — coined the Fourth Industrial Revolution and characterized by rapidly evolving and disruptive advances in technology — has created a new and intimidating...
In this special report, we explore how virtualization can provide significant advantages for deploying process control systems at pharmaceutical plants.
Discover how peptone composition influences microbial growth, vaccine yield, and consistency—unlocking the science behind more reliable veterinary vaccine production and improved...
Discover evidence-based insights on the evolving veterinary vaccine landscape—covering mRNA innovations, antimicrobial resistance, and the global data trends shaping animal health...
Explore how innovative vaccine development and optimized peptone mixes are shaping a healthier future for animals, humans, and the planet through the One Health approach.
Quotient Sciences' facilities in Philadelphia, PA offer flexible, phase-appropriate drug product development and scale-up, extending through to reliable commercial drug product...
Quotient Sciences balance clinical, CMC, and regulatory requirements to help you accelerate your drug product to commercial manufacture with ease, even in cases where you may ...
Discover how Smart Visual Factories are reshaping pharmaceutical manufacturing with AI-driven vision, real-time monitoring, and predictive control. Explores the future of intelligent...
Advancements in cleanroom technology are redefining pharmaceutical manufacturing with energy-efficient HVAC, sustainable materials, and intelligent airflow. However, much more...
Learn about the role of environmental monitoring in a robust contamination control strategy to maintain product integrity and safeguard patient safety.
Explore proven alternatives to fetal bovine serum (FBS). Discover how donor bovine serum and other options can reduce cost and supply risks while maintaining performance in bioproductio...
This eHandbook explores what companies can do to prepare for these challenges as well as the opportunities to mitigate the impacts, including the use of technology such as artificial...
Uncontrolled humidity creates problems in every step of pharmaceutical manufacturing. From R&D labs, to production, packaging, and distribution — moisture can damage product and...
Learn how a fast-growing CDMO streamlined buffer preparation, reduced costs, and avoided $5.1M in CapEx/OpEx—while saving 56% in prep time. Discover proven strategies to overcome...
Explore how to overcome cost, quality, and scale-up challenges in buffer preparation. Learn when to outsource, reduce risk, and streamline processes to accelerate biopharmaceutical...
Discover how to reduce hidden costs, minimize risk, and streamline buffer preparation workflows. Learn how outsourcing solutions can improve efficiency, ensure consistency, and ...
With manufacturers under increasing pressure to reduce costs, enhance compliance, and accelerate production timelines for high quality drugs, they are increasing their investments...
Sustainability is shaping the future of pharmaceutical manufacturing and smarter, greener, and faster sustainable packaging solutions are a big part of the evolving landscape....
Discover how Aquafine® UV systems offer a compact solution ideal for pharmaceutical water treatment. Delivering ultra-low residuals, minimal downtime, and compliance with stringent...
Discover how automated calibration improves compliance, reduces human error, and increases efficiency in pharmaceutical manufacturing. This Beamex white paper explores the benefits...
Unlock the full potential of your GMP assets. Discover how life sciences organizations can optimize reliability, compliance, and performance with a data-driven approach to Asset...
Three of Cognite's chemical, refining, and energy customers take center stage in this product tour video that showcases why and how they are transforming their operations.
Are you making quick-enough progress on your industrial Gen AI journey? Learn what it actually takes to trust, deliver, and scale across operational use cases.
Optimize safety, efficiency, and compliance in biopharma fluid handling with this essential guide to managing single-use bioprocess bags. Learn how modular, ergonomic, and contamination...
Contract development and manufacturing organizations (CDMOs) are more critical than ever to the biopharmaceutical industry, providing essential outsourcing services to customers...
Explore how real-time TOC sensors are transforming pharmaceutical water systems by delivering continuous monitoring of organic contaminants, ensuring compliance and safety. With...
Blending and tableting create hazardous dusts. Learn how dust collector filters reduce exposure—download our eBook about media that is best for each dust type.
Pharmaceutical manufacturing hinges on the production of purified water that meets strict pharmacopeia regulations. To ensure consistent water quality, real-time monitoring is...
Take corrective action before a system goes out of specification, ensuring that your processes remain streamlined and compliant. With continuous insights at your fingertips, you...
Regulations in the pharmaceutical industry are constantly increasing— and navigating them doesn’t have to be overwhelming. Discover a real-world example using continuous TOC monitoring...
Read more about how WarmMark QR addresses today’s common cold chain monitoring challenges through an innovative combination of visual and digital tracking.
