05.15.25 -- A Facilities Expert Answers Audience Questions On Construction And Validation

The industry is on the verge of a digital revolution. Find out how to navigate the digital revolution with a digital maturity assessment to guide digital transformation, efficiency, and sustainability.

The biopharma industry leverages Genedata Profiler to integrate, curate, and analyze diverse R&D data, enabling collaborative, compliant, and AI-driven translational research to optimize drug development.

Automating your bioprocessing workflows can significantly improve quality and scalability. To reap the benefits, implement plant-wide control software that enables seamless integration and efficiency.

Monitor assets in real-time, anticipate issues, and maintain optimal performance effortlessly by exploring a cloud-based asset monitoring platform that offers proactive support and rapid response from experts.

Discover how organizations must continuously reassess validation processes and digital tools to ensure compliance, enhance efficiency, and support global scalability amidst evolving regulatory expectations.

Gain deep insights and practical guidance for data by exploring how an industrial DataOps hub offers data contextualization and standardization, driven by evolving customer needs to leverage data models.

A pharma company faced a 4% yield drop and variability at a manufacturing facility. Explore how they leveraged an AI-based platform to unify data, pinpoint inefficiencies, and enhance consistency in yields.

Single-use (SU) systems and components are growing in demand as they offer minimal contamination risk. Review a standardized SU assembly for bulk-fill processing that aims to improve efficiency.

Filtration removes contaminants to ensure safety and is essential in various applications, from lab-scale tasks to GMP production. Explore how its simplicity and reliability make it indispensable.

Explore the reasoning behind the increasing demand for cleanroom technology as well as the advantages modular cleanroom design brings to the sterile processing of complex therapies.

Reduce the time and risks involved in maintaining a traditional bioreactor with this single-use solution for biopharmaceutical manufacturers.

In this session, an expert walks you through the purity testing process and explains identification methods for biological indicators to help end users.

Compare manually washed labware and labware cleaned in automatic washing systems, to see how the challenges of manual washing can impact your labs efficacy and repeatability.

Learn how thorough cleaning and process optimization prevent cross-contamination, ensure product integrity, and enhance efficiency while also improving compliance and reducing costs.