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Pharma & Biopharma Learning Center
Producers of pharmaceuticals and biologics are challenged to become more efficient in discovering and developing candidate drugs while increasing manufacturing productivity and reducing costs. Advanced instrumental techniques and workflows can help to accelerate the development pipeline and optimize production processes.
Thermo Fisher Scientific has innovative solutions at every stage of the bio/pharmaceutical process; from discovery through to production and QC. Our deep understanding of the challenges faced by producers of medicines allows us to forge partnerships that deliver next-generation drugs to market quicker.
Pharma & biopharma learning center features
Application note
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.
eBook
Ultra high-pressure liquid chromatography has become an important analytical tool for meeting these varied needs for higher throughput. Analytical instrument makers believe that further advances in the technology will enable UHPLC to have an even bigger impact on the pharmaceutical industry.
White paper
Accounting for the inherent heterogeneity of monoclonal antibodies is essential to ensure production of consistent and safe therapeutics and, in light of this, there is an array of chromatographic and supporting regulatory systems.
Brochure
Four simple workflows to allow you to understand the form, site, & variation of glycosylation on biotherapeutic proteins.
Mobile app
Discover our range of products and workflows dedicated to biotherapeutic characterization. From discovery to lot testing, and from aggregate analysis to peptide mapping, we have the solutions you need.
eBook
This eBook offers guidance and best practices for the issues that concern the pharma and biotech manufacturing industry the most.
Videos
Extractables & Leachables: Overview
E&L analysis overview of differentiated solutions to increase sample throughput, streamline workflows, and increase confidence in results.
Extractables and Leachables: Challenges and Solutions
E&L challenges & Thermo Scientifics differentiated solutions to increase sample throughput, streamline workflows, and increase confidence in results.
Pharma & biopharma learning center subtopics
Biopharmaceutical Characterization Information
In recent years biopharmaceuticals (pharmaceuticals manufactured by biotechnological methods) have become successful medicinally and commercially.
Drug Discovery & Development Information
Modern drug discovery is the convergence of several scientific disciplines to find new medicines to cure disease or relieve suffering. The pharmaceutical pipeline is filled with approximately 5,000–10,000 drug compounds to only one approved commercially available drug.
Pre-Clinical and Clinical Drug Testing Information
In pharmacokinetic studies, bioanalysis method validation is crucial to minimizing random error and systematic bias, which ensures quality of analytical results. Bioanalytical method validation is a controlled procedure that comprises all the vital steps to establish that a certain method is capable of producing accurate, dependable and reproducible results that are appropriate for a specific analytical application.
Pharmaceutical QA/QC Information
Modern advances in pharmacology have resulted in increased life expectancy and reduced suffering of patients fighting disease. It is the frail and vulnerable that have come to rely on modern medicines. Consequently, it is paramount that prescribed drugs have the desired therapeutic efficacy, without fear of harmful side effects from impurities. For healthcare systems to provide quality care, prescription medicines must meet regulatory quality assurance standards.
Pharmaceutical Data Management Information
Regulatory inspections of pharmaceutical companies are increasing. Integrated informatics solutions allow you to provide evidence that your GMP processes are validated, that you are using appropriate resources, and that your analytical data are accurate, complete, and consistent. You can be sure that you have full data integrity, processes are managed according to 21 CFR part 11 requirements, and that your audit checklist will satisfy the inspectors.
Pharmaceutical Manufacturing Processes and Production Information
Learn about solutions to improve manufacturing processes, save time, improve processes, protect brand integrity, and help ensure patient safety in the pharmaceutical and biotechnology industries.
Interested in the analysis of nitrosamines in pharmaceutics?
Download the latest applications notes, register for the latest webinars, and learn more about the analysis of nitrosamines and their precursors.
Related Products
Lab ideas for medicine makers – current topics for pharma – biopharma analytical labs!
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.
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