03.20.25 -- Why You Should Consider AI-Powered Digital Twins For Smart Manufacturing

Learn how digital standardized tools can simplify your scaling practices, help you better predict and visualize scaling needs, and reduce trial-and-error experimentation.

Gain insight into how a leading pharmaceutical company identified the root cause of long-standing inefficiencies, optimized performance, and productivity with unprecedented speed and accuracy.

Discover how Kaneka Eurogentec, a leading provider of custom DNA synthesis and molecular biology service, enhanced their fragment analysis to achieve higher efficiency and accuracy in their workflows.

Embrace the transformative power of predictive modeling and digital twin technology to optimize bioprocess efficiency, ensure product quality, and drive innovation in biopharmaceutical manufacturing.

The peptide manufacturing industry is evolving to meet the demands of efficiency, scalability, and sustainability. Find out how the latest innovations are addressing these challenges.

Read about how to dissect the potency assay development process into its key steps, which offers a clearer understanding of the journey.

Symmetry Surgical enhances operations and quality management using software to improve efficiency, compliance, and data-driven decisions while producing over 2 million surgical devices annually.

Attain knowledge about a differential scanning calorimeter that offers thermal stability screening of buffer formulations and protein sequence modifications.

See why CMOs and CDMOs who do not address the rising demand from life science clients for greater visibility in the manufacturing process risk falling behind.

In the age of digital transformation, AI is no longer optional. Explore how to successfully integrate AI into your organization's operations for a competitive edge.

Uncover how reality capture was used to create a digital twin 750,000-square-foot Pfizer campus to support asset reinduction to Maximo EAM, which saves Pfizer 3,000 hours per year.

Review how digitalizing commissioning, qualification, and validation (CQV) with a new software streamlines processes, enhances compliance, and reduces time to drive efficiency and sustainability.

The first step towards IT-OT collaboration is getting these functions to speak the same language. Here, we outline key Industrial DataOps terms and aim to establish a common dictionary for IT and OT.

Life sciences startups must integrate compliance early to ensure regulatory approval, and trust. Prioritizing compliance streamlines processes, and enables long-term success.

Explore strategies for accommodating the ever-increasing upstream titers and volumes to prevent downstream purification from becoming a bottleneck.

Current advances in cell, gene, and tissue therapies require a rethinking of how—and where—cleanroom manufacturing facilities could be built, which enables more options for sponsor process control.

Learn about liquid submersible biological indicators (LSBI), including the three basic LSBI formats, and how caramelization due to long sterilization cycles affects the media's ability to promote spore growth.

Determining the best single-use systems to implement in a given manufacturing operation requires a thorough understanding of both the process specifications and the capabilities of the component.

Acquire a thorough understanding of environmental monitoring, covering the fundamentals of particle counting and cleanroom designs, regulatory expectations regarding market release, and more.

Single-use systems are critical to sustainable virus filtration. Discover a guide that will lead you to select the right equipment and outline the best practices for implementation.

Gain insight into the role of single-use technology in advanced therapy manufacturing, why pharmaceutical manufacturers are switching to disposable technology, and more.

Examine the significance of minimizing particulate contamination in pharmaceutical and biopharmaceutical products produced through the use of single-use systems.

Uncover labware cleaning techniques, comparing manual and automated processes, and how balancing the four factors of the Sinner’s Circle ensures effective, repeatable laboratory outcomes.