12.19.25 -- M&A In GLP-1 Technology: Practical Recommendations And Best Practices

Engineering controls designed to mitigate exposure and create separation between the operator and toxic material are available in many forms, all with their own unique advantages and risks.

Discover how automation, analytics, and AI are driving smarter process intensification and enabling a shift toward connected, continuous manufacturing.

Explore five key factors that drive a seamless and efficient technology transfer, highlighting how a culture of technical expertise, customer focus, and operational flexibility is crucial to success.

Realize the value of connectivity, and more specifically, the value of the information provided by checkweighing, metal detection, vision inspection, and X-ray inspection.

A one-site CDMO streamlines drug development by co-locating R&D, GMP, and manufacturing. This integration accelerates tech transfer and decision-making, significantly compressing project timelines.

Gain insight into smoke studies that help visualize airflow in cleanrooms, ensuring aseptic conditions and regulatory compliance for sterile production, especially on new aseptic filling lines.

A recent project applied process improvement methodology to the process validation step that ultimately provided not only an optimized, robust process but also an economic advantage.

In the CCIT space, one single inspection technology cannot be used for every type of pharmaceutical product. You should always weigh the various factors to determine the ideal inspection methodology.

Reconstructed nasal epithelium and CT-based 3D nasal casts provide more predictive, physiologically relevant models for assessing nasal drug delivery, improving accuracy in formulation development.

Optimize your TFF process with single-pass technology by joining experts Mike Dango and Michael Brauchle as they share key strategies for scalable, efficient filtration process development.

Spray dry technology is being leveraged to create shelf-stable, dry-powder vaccines to treat and prevent the spread of tuberculosis which could significantly improve our global response to disease.

Steven Facer and Laxxon Medical COO Klaus Kühne describe the capabilities of 3D screen printing for pharmaceutical production. Explore prototyping, IP protection, release profile possibilities, and more.

Find out how leading Biotech teams are eliminating SharePoint headaches, streamlining document reviews, and accelerating submission timelines without the chaos of version confusion or email overload.

Validation in GxP environments is often the bottleneck in digital transformation—manual, repetitive, and complex. One company's Intelligent Agents are transforming that process.

We discuss the trends in new molecular formats, which is one of the current drivers of renewed interest in fermentation technologies, along with some of their challenges. 

Learn more about a solution that ensures particularly efficient and reliable vertical and horizontal form fill and seal machine labeling.