Thermo Fisher Scientific has innovative solutions at every stage of the bio/pharmaceutical pipeline: discovery, development, clinical, manufacturing, and quality control. Our deep understanding of the challenges faced by producers of medicines allows us to forge partnerships that more quickly deliver next-generation drugs to market.
Cells, proteins, target based assays, and services to drive efficiency in assay development, screening, and metabolic and safety assessment.
Robust products and workflows for therapeutic protein characterization from discovery to QC.
Robust products and workflows for small molecule drug assays and impurity analysis.
Identify and quantify drug metabolites with greater speed, sensitivity and confidence.
Single use technologies (SUT), labware, media, purification, and analytics for drug products, impurities, and contaminants.
Advanced tools for cancer research, including; cell analysis, transfection, epigenetics, genomics, and biomaker analysis.
Validated solutions for pharmaceutical microbiology laboratories, including; media, containers, labware, and environmental monitoring.
Compliant data acquisition and management informatics solutions, including; enterprise CDS, LIMS and SDMS.
Easily obtain fast, accurate material verification for immediate release of raw materials into production.
Solutions for scaleup and continuous processing, including extruders, rheometers, compounders, spectrometers and granulators.
Process analytical technology solutions for increasing productivity, improving quality assurance and control, and reducing operating costs in pharmaceutical development and manufacturing.
A single platform to track and manage data across samples, assays, processes, requests, and inventory. Our laboratory data management solutions track and manage data throughout the therapeutic discovery and development processes—from antigen generation to downstream bioprocessing and translational programs.
The Platform for Science is an underlying data management infrastructure designed to support workflows across your scientific organization. This flexible, extensible, cloud-based platform helps you easily collect, store, access, share and use your scientific data.
High-quality raw materials designed for oligonucleotide (ASO, siRNA, etc.) and mRNA synthesis from research, clinical development to commercialization.
This application note discusses the importance of proper sample preparation for mAb subunit analysis and to provide optimized LC/MS conditions to achieve conclusive information on the mass of the subunits as well as for performing middle-down analysis for sequence confirmation.
Save time, improve processes, protect brand integrity, and ensure patient safety, from raw material identification through the pharmaceutical manufacturing process, to finished and packaged pharmaceutical product inspection.
Developing robust quantitation assays is possible with both Triple Quadrupole and Orbitrap-based High- resolution MS instruments. Both technologies enable confident quantitation in a variety of sample types.
Our LC-MS on-demand webinar series expands your application knowledge for pharma, biopharma, environmental, omics, food, forensics and clinical research and more. Learn how the latest high-performance mass spectrometry solutions can enable your laboratory to solve your most pressing analytical challenges, regardless of sample type.
Our wide range of solutions are an important resource to quickly and accurately monitor your drug as it moves through the development workflow but also enables quality and regulatory compliance through the drug formulation, development and manufacturing processes. Our solutions empower you to quickly confirm the safety of your drug at every stage of development using the following techniques.
Lab ideas for people – like yourself– in analytical labs making medicines, directed by topics, ideas and thoughts from your fellow medicine makers. Each month, a new theme addresses challenges and solutions around technology and workflows.