Articles

Improving AAV Vector Quality with In-Process Monitoring of Capsid Formation

Fast path to market: Going from GMP1 to PPQ in just 12 months

As today’s labs continue to evolve, the software solutions that support them
must too. Likewise, laboratory and organization leadership must be open to the
advance-ments available to them from modern technologies. In this white paper, learn
how a SaaS-based LIMS modernization program optimizes data management, fosters
collaboration, and improves decision-making to stay at the forefront of scientific
innovation.

Transfer Responsibility with SaaS: Trade Outdated LIMS Technology and IT Hassles for Zero-touch Maintenance

The efficiencies and insights of artificial intelligence (AI), machine learning (ML), predictive analytics, and other emerging technologies offer abundant opportunities to laboratories. To help customers leverage digital transformation and prepare for the lab of the future, LabVantage Solutions has devised a five-step process for successfully implementing and profiting from AI in the lab.

Five Key Steps to Successful AI in the Lab (Dec 2024)

Illuminating industry trends, challenges and sentiments

The Pulse: Global R&D Insights in Biopharmaceuticals  

Stay compliant with Annex 1 for early phase sterile fill finish processes. Discover how to implement robust contamination control strategies, integrate isolator technology, and conduct integrity testing to meet stringent European Union standards. The guide provides a comprehensive look at key elements such as PUPSIT, critical zone controls, and monitoring and training for aseptic processes.

Navigating Annex 1 for Early Phase Sterile Fill Finish in Clinical Supplies

Explore the complexities of gene and cell therapy development with our comprehensive guide to Chemistry, Manufacturing, and Controls (CMC) testing. Learn how our expertise ensures the safety, potency, and quality of advanced therapies, supporting your journey from product development through regulatory approval.

Your Ultimate Guide for CMC Testing Support for Gene and Cell Therapy

Raw Materials are the foundation of every biopharma product. Our
ultimate guide highlights how our testing support can help you establish purity, identity,
and quality standards, ensuring a smooth manufacturing process and adherence to
regulatory requirements.

Ensuring Quality from the Start: Raw Materials Testing Support

Elevate your viral screening with Eurofins BioPharma Product Testing’s qPCR- based assays. Our advanced testing goes beyond standard screenings to detect even dormant and hard-to-detect pathogens, ensuring comprehensive safety in every stage of the allogeneic therapy pipeline. Protect your products – and your patients- with industry-leading sensitivity and specificity. 

Ensure the Safety of Allogeneic Therapies with Advanced qPCR Testing

Spray drying enables the production of amorphous solid dispersions, allowing efficient scale-up
from small screening batches to commercial levels. By leveraging small-scale experiments for process design
and qualification, a robust validation strategy can be developed to support flexible, scalable manufacturing for
small-molecule drug products. 

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