In this eBook, you will gain insights on: Sharpening pharma's data integrity with automation The top 10 most digitally innovative pharma companies Building the next generation...

X-Ray Fluorescence (XRF) technology streamlines elemental impurity screening, offering faster, cost-effective, and resource-efficient alternatives to traditional ICP methods in...

Proper and thorough monitoring of pharmaceutical water systems is imperative to prevent undetected issues from shutting down production and to deliver the highest quality products...

A fundamental aspect of pharmaceuticals manufacturing is the production of purified waters that meet pharmacopeia regulations. For continuous assurance of water quality, on-line...

Discover the power of Flow Imaging Microscopy in biopharmaceuticals. Learn how FIM works and how it can uncover details in your samples, enhancing the characterization of API ...

Supply chain challenges have long been a reality for pharma manufacturers, but the pandemic underscored the critical need for enhanced visibility and control. Added pressures,...

A collective analysis of reshoring efforts across several major manufacturing industries

Discover how simplifying pneumatic circuits enhances drug production efficiency, quality, and control in the growing life sciences market.

In the modern pharma landscape, packaging is more than just a protective barrier for drug products. Effective packaging ensures drug quality, complies with traceability regulations...

Enhance your bioproduction with Gibco™ Efficient-Pro™ Medium and Feed systems, achieving increased productivity in CHO-K1 and CHO-S cells. Experience reduced variability and superior...

Elevate your CHO cell culture productivity with the Gibco™ Efficient-Pro™ Medium and Feed System. Download our application note to explore how the Efficient-Pro™ Medium and Feeds...

Ready to Transform Your mAb Manufacturing Workflow? Enhance productivity and efficiency with our advanced Efficient-Pro™ media and feed systems​

Major players in the pharmaceutical industry are embracing digitalization – calibration processes, however, are still largely paper-based. This results in operational inefficiencies...

Get your free maintenance guide to help prevent pests in your facility.

This article shares five top considerations when selecting a cell culture media supplier for a catalog medium or custom formulation manufacturing. Learn ways to maximize confidence...

Upholding rigorous quality standards is not only a regulatory imperative but also vital for ensuring the efficacy and safety of pharmaceutical products. And as many pharma manufacturers...

Nine out of 10 Fortune 500 executives surveyed expressed interest in the idea of outsourcing energy operations to reduce risk. Learn how an Energy as a Service model can support...

Discover insights into FDA's Data Integrity Guidance and how to leverage the Cloud to achieve GMP compliance.

Discover how Blue Mountain's Regulatory Asset Manager (RAM) propelled AmplifyBio, a leading Contract Research Organization (CRO), into a paperless future.

Leverage the latest advancements in technologies to drive innovation and deliver improved patient outcomes.

mRNA-LNP manufacturing is fraught with obstacles, resulting in higher program risk, inflated costs, and delayed market release. With the right knowledge, companies can overcome...

During tableting processes, APIs become airborne. These dust particles can harm workers, reduce air quality, contaminate products and cause explosions. Learn how dust collectors...

Advanced chemical indicators give you the peace of mind that comes from reliable insights into your supply chains.

Learn how digitalization can drive 24/7 success in your facility with our newest white paper.

Considerations for obtaining optimal results in laboratory and medical devices

Are purification strategies for mAbs moving you forward, or holding you back?

Vacuum technology plays a crucial role in pharmaceutical processes (conveying, inertization, distilling, and drying). Using the most efficient vacuum technology can make these...

Learn the process and results of a two-phase scale-up strategy that was used for three complex dry powder medium products.

Challenges can arise when transitioning a media formulation from a non-cGMP prototype to a cGMP-manufactured product. Our case study outlines the scale-up process that was used...

Considering scalability, cost effectiveness, and convenience is essential to find a media format that can meet your current and future needs. Read our article to learn more about...

Scale-up is a critical stage, with an optimized medium and robust supply chains being central to consistent product quality and a cost-effective process. Read our article to discover...

A Contract Manufacturing Organization that produces and packages pharmaceuticals for customers which are then distributed in more than 150 countries found a solution to supply...

A collection of the most-read feature articles of the year, chosen by the Pharma Manufacturing digital audience.

Operational technology (OT) risks are on the rise, with more threat actors and incidents targeting manufacturers by the day. Even when organizations invest in preventative OT ...

Download this IDC InfoBrief to uncover key drivers and challenges pharma organizations face, as well as how investing in Edge Computing can help companies reach their operational...