06.26.25 -- How Modular Facility Design Can Accelerate GMP Facility Construction

Process optimization is key to achieving effective pharmaceutical and cosmetic critical cleaning. Learn how manufacturers can improve cleaning efficiency and ensure product safety.

Gain insights into the nuances of cleanroom conceptual design for GMP operations and learn how an integrated approach can ensure regulatory compliance, functionality, and environmental performance.

Single-use strategies and tools are constantly evolving to better serve industry needs, and adept solutions providers can help streamline development with simple, custom adaptations.

Single-use technology is vital for ensuring the quality and expedited market entry of genomic medicines. Learn how LNP technology is paving the way for a new era of personalized, precise medicine.

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

This Q&A addresses attendee questions from a recent webinar about a new biomanufacturing site in Waltham, MA, equipped with state-of-the-art equipment.

Discover how digital transformation is revolutionizing industrial operations with smart technologies and data modeling to help optimize production, predict failures, and enhance quality.

Biomass soft sensors utilize existing measurements from hard sensors to predict biomass levels in real-time. Explore how to enhance your bioprocessing production, decision-making, and efficiency.

A successful large-scale public health emergency response requires adaptable manufacturing capabilities, an experienced workforce, and effective private-public partnerships.

Learn about multivariate data analysis (MVDA) techniques, like PCA and PLS, that enable near real-time monitoring, prediction, and optimization of biomanufacturing processes.

Is your company still using outdated methods for its QMS? It's time to evolve. Uncover how an integrated QMS can streamline operations, enhance compliance, and support your company's growth.

The biopharma industry must shift from data collection to process knowledge, leveraging digital tools to optimize drug development, enhance quality, and streamline tech transfer through digital maturity.

From automating tasks to optimizing complex processes, AI is reshaping biopharmaceutical manufacturing. Discover how AI is moving beyond trends to become a foundational element in the industry.

Delve into the advancements and transformative impact of mRNA vaccine technology on modern medicine and explore how this technology is revolutionizing healthcare for the future and beyond.

Discover how to optimize membrane proteins for cryo-EM. Experts reveal a data-driven workflow using NativeMP Copolymer Technology and a multi-parameter tool for detergent-free stabilization.

Examine why organizations must integrate data and processes to enhance quality and insights to improve operational efficiency, patient health, and regulatory compliance.

Explore the PDA Pharma Digitalization Survey and key challenges in pharmaceutical digitalization, including budget constraints, data security concerns and resistance to change.

Join our webinar to explore how Genedata Profiler and Leica Aivia AI-powered tools streamline biomarker discovery, enhance data analysis, and improve research efficiency in personalized medicine.

Are you overwhelmed by paperwork during validation projects? Discover how AI-enabled validation can streamline operations, strengthen compliance, and keep you ahead in the fast-paced pharmaceutical and biotech industries.

Integrating advanced digitalization solutions and prioritizing data security can accelerate drug development while reducing costs and ensuring consistency across a global network.