04.03.25 -- Retrofitting Facilities For Modern Bioprocessing And Pharma Production

Explore four common applications of cryopreservation and the science behind selecting the appropriate materials to build single-use solutions that enable cryogenic storage for cell and gene applications.

As pharma companies aim to overcome development obstacles, it is important to incorporate GMP expertise alongside novel technologies that can enhance the properties of APIs and dosage forms.

Learn about three of the best methods for cleaning proteins, RNA, and DNA from laboratory equipment.

Ensure precise, validated cleaning processes for your pharmaceutical projects, minimizing downtime and mitigating drug shortages that stem from manufacturing interruptions.

Single-use systems are increasingly prevalent in biotechnology processes. Explore the benefits, challenges, and solutions presented by modular single-use systems.

How does the UFMini single-use centrifuge significantly reduce filtration needs and enhance the amount of viral titer collected?

A PDA survey reveals moderate digitalization in pharma, highlighting gaps in advanced integration. Explore how Aizon Execute accelerates digital transformation with solutions for Pharma 4.0 readiness.

Learn how a CDMO automatically created a comprehensive batch report model to drive their reporting and speed root cause identification of quality failures with an Industrial DataOps software solution.

Find out how cloud solutions empower businesses to achieve agility and security in their digital transformation journey, and explore key considerations and insights from real-world success stories.

Traditional corrective action processes can obstruct continuous improvement. See how advocating for streamlined procedures, risk assessment, and a culture of learning enhances organizational efficiency.

Explore the digital evolution of manufacturing control and management, the building blocks of Pharma 4.0, and how the life sciences industry can realize the full potential of Pharma 4.0.

Quality management in life sciences is crucial for optimizing patient health. Learn how modern quality management systems optimize patient outcomes, enhance safety, and drive operational efficiency.

Equipment validation ensures pharmaceutical equipment meets regulatory and quality standards. Explore how a structured process ensures compliance, reliability, and high product quality.

Automation enhances efficiency and minimizes contamination risks and labor costs. Despite the initial investment in automation equipment, the long-term savings can be significant.

See how a global biopharmaceutical company transitioned from a paper-based Quality Management System to an automated solution to enhance efficiency and compliance in change management.

Asian pharma manufacturers are constantly under pressure to produce high quality products on time. Explore how these companies are leveraging MES to enhance efficiency and compliance.

Learn how AI is transforming the biomanufacturing industry and how partnerships between pharmaceutical companies and academic institutions are poised to set the new standard.

Discover how integrated solutions create a harmonious bioprocess ecosystem. Learn about data integration, digital technologies, and automation to streamline your lab workflow and drive innovation.