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Biopharmaceutical Formulation Stability Solutions

Biopharmaceutical Formulation Challenges and Stability Solutions The biopharmaceutical revolution has fundamentally transformed therapeutic medicine, with protein-based therapeutics including monoclonal antibodies, fusion proteins, antibody-drug conjugates, and advanced biologic systems becoming cornerstones of treatment for cancer, autoimmune diseases, metabolic disorders, and numerous...

Biodegradable Films in Pharmaceutical Packaging

Eco-Friendly Biodegradable Films Transforming Pharma Packaging The pharmaceutical industry stands at the forefront of a packaging revolution, with biodegradable films in pharma packaging emerging as transformative solutions that address both environmental sustainability and product protection requirements. These innovative materials represent...

Artificial Intelligence in Pharmaceutical Process Control Trends

Artificial Intelligence in Pharmaceutical Process Control: What's Now and What's Next The pharmaceutical manufacturing landscape is undergoing a transformative revolution as artificial intelligence in pharmaceutical process control emerges as a cornerstone technology for next-generation production facilities. Industry leaders are witnessing...

Overcoming Scale Up Bottlenecks in Cell Culture Bioprocesses

Overcoming Scale Up Bottlenecks in Cell Culture and Downstream Processing In the rapidly evolving landscape of biopharmaceutical manufacturing, the journey from laboratory-scale success to commercial production represents one of the most challenging phases in bringing life-saving therapies to patients. Scale...

Sapio Sciences and Ultima Genomics Partner to Advance Multi-Omics Research

Partnership delivers global, end-to-end solutions to accelerate genomics research Sapio Sciences, the science-awareTM lab informatics platform, today announced a strategic partnership with Ultima Genomics. The collaboration will make multi-omics workflows more accessible and streamlined for researchers by integrating Sapio’s AI-powered lab informatics...

Optimizing DMF Quality for Successful Health Authority Filings

A Drug Master File (DMF) is a confidential regulatory submission that provides comprehensive, precise, and accurate data about an Active Pharmaceutical Ingredient (API) or a Finished Product Dosage Form (FP). It encompasses critical information on the manufacturing process, quality...

The Shift Towards Real-World Evidence Clinical Development

The fact remains that the pharmaceutical spectrum happens to stand on the edge of fundamental transformation as the real-world evidence clinical development methods go on to reshape how one gauges the therapeutic intervention. This kind of revolution happens to...

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