All Thermo Fisher Scientific articles
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ArticleBuilding the foundation for the orchestrated lab of the future
As pharmaceutical laboratories face mounting pressure to accelerate timelines and manage growing data complexity, intelligent laboratory operations underpin the next generation of connected, autonomous lab environments.
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ArticleLipid formulation development: why softgels are the technology of choice
With their improved bioavailability and a straightforward manufacturing process, innovative lipid formulations such as softgels offer an attractive alternative to common oral solid dosage (OSD) forms like tablets and capsules, helping to streamline drug development.
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WebinarOptimising efficiency and yield through bioprocessing automation
Watch this webinar to explore how process Raman spectroscopy supports bioprocessing automation across upstream and downstream workflows, helping teams increase yields, improve process efficiency, and ensure more consistent product quality.
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WebinarSmarter Raman QC for biopharma fill-finish with scalable model transfer
Join this webinar to explore how modern Raman spectroscopy is transforming biopharma fill-finish quality control through faster analysis, multi-attribute insight, and scalable model transfer.
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WebinarLipid formulations in softgels - enhancing bioavailability and therapeutic efficacy
This webinar will explore how lipid formulations in softgels can enhance drug absorption and bioavailability.
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WebinarControlling impurities in pharmaceutical waters
This virtual panel explores impurity control in pharmaceutical waters, the differences between microbial and organic contaminants, and best practices for measurement and treatment.
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ReportPharma Horizons: Artificial Intelligence
EPR’s latest Pharma Horizons report explores the latest advances in artificial intelligence (AI) for drug and clinical development, regulation and more.
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WebinarLeveraging early insights to accelerate the oral drug development cycle
This webinar explores oral drug product development and how to address critical challenges such as complex formulations and regulatory hurdles.
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WebinarSafety reporting in clinical trials: six core considerations for success
This webinar will provide guidance in navigating the terrain of pharmacovigilance, including regulatory challenges, and gain a deeper understanding of the pivotal role played by safety reporting in clinical research.
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Articleebook: Twin-screw extrusion for pharmaceutical applications
This compendium explains how hot-melt extrusion can help overcome common challenges in pharmaceutical development, with guidance on all stages of the HME process from formulation characterization to process design/development, and downstream processing.
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Webinar
Enhancing biopharma workflows with the power of UV/Vis spectroscopy
Discover the valuable role ultraviolet-visible spectroscopy can play in quickly and accurately monitoring a drug as it moves through the research & development workflow and enabling quality and regulatory compliance through the manufacturing process.