PRODUCTION
Improve The Bioavailability Of Poorly Soluble Drugs
KinetiSol is a fusion-based, solvent-free process that utilizes frictional and shear energies — in a fraction of the time of other amorphous solid dispersion technologies.
mAb Up- And Downstream Process Intensification Strategies
Discover how to reduce monoclonal antibody (mAb) manufacturing time and costs through process intensification. Learn about continuous perfusion, ultrahigh cell density banks, and more.
Key Functions Of The ÄKTA Oligosynt Synthesizer
Discover a compact, fully automated oligonucleotide synthesizer for robust, scalable process development. Learn how it can help establish a robust and reproducible oligo synthesis process.
Single-Use Technology For Quality mRNA Manufacturing
Learn how single-use technologies deliver important benefits for mRNA manufacturing, including increased speed, quality, flexibility, and adaptability to different dosages and scale-up strategies.
Accelerating Progress: Key Considerations For CDMOs To Maximize Productivity And Scalability
Due to the urgent demand for vaccines and treatments, the biopharmaceutical industry is experiencing disruptive changes and increased demand on resources that are requiring a significant operational transformation. To accelerate the delivery of life-saving therapeutics, i...
Scaling Up A Revolutionary Amorphous Solid Dispersion Platform
Process parameter and quality attribute relationships, including those for typical pre- and post-ASD unit operations, will be explored in the context of real-world examples.
Your Contract Manufacturer Partner
Discover an integrated solution for pharmaceutical companies that offers a broad range of manufacturing services and capabilities to produce high-quality devices.
Thermo Fisher Scientific Suzhou, China Manufacturing Site Capabilities
Watch this video to learn more about this manufacturing site capabilities, quality management systems, PPI implementation, product expansion, assurance of supply and lead times.
How To Plan For Trouble-Free Filter Validation
Watch to learn when filter validation should be performed, what is required from an end user and laboratory testing perspective, and how to achieve first-time success for various drug products.
Challenges And Solutions In Aseptic Connection And Disconnection
Progressive biomanufacturing processes require advanced tools to reliably connect and disconnect components. Here, we show a wide range of connection and disconnection options.
Intensification Strategies For Upstream, Downstream Processes
How do you know if an intensification approach will provide advantages? Three process intensification experts show how various intensification approaches affect outputs using different scenarios.
Showcasing A Scalable Downstream Platform For Multiple AAV Serotypes
Watch to explore how to maximize AAV full capsid recovery, establish a scalable platform for various serotypes, and utilize analytical tools to measure empty/full capsid ratios and AAV titers.
Improve The Performance Of Your Small And Large Molecule Medicines
Explore the latest in nanotechnology advancements including recent clinical data, formulation applications, and API optimization to NanoImprove formulations.
Challenges Of The IVT Reaction In mRNA Production
mRNA synthesizes from the plasma template in the in vitro transcription (IVT) step. Learn tips from a principal scientist for optimizing the IVT step of mRNA production and purification.
Simplify Your Downstream Calculations With Bioprocessing Downstream Calculators
Simplify complex biopharma downstream processing tasks using a suite of powerful, web-based calculators designed to streamline workflows and automate intricate mathematical modeling.
Ensure Speed And Success With Your Drug Delivery Project
Hear from experienced professionals in the drug delivery space on how to ensure success and speed-to-market by establishing a firm foundation when working with a CMO.
Rapid Process Development And Technical Support For AAV Scaleup
Accelerate your AAV production journey. Learn how rapid process development and expert support can streamline your path from vial to purified bulk, ensuring scalable and efficient manufacturing.
Workflow For Rapid Sterility Testing
Learn about the workflow for an automated solution for the rapid detection, imaging, and quantification of viable microbial contaminants in filterable samples at various stages of the manufacturing process.
Modular Assembly Equipment For Flexible And Scalable Solutions
Every assembly line is different. And every company has individual requirements. Learn why modularity is necessary streamline your drug delivery device assembly operations.
How To Select Your DSP Chromatography Technology
Watch to explore the differences between the conventional single-column batch method and the multi-column approach for mAb capture.
Thermo Fisher Scientific Customer Testimonial - Libbs
An overview of Libbs product portfolio and how they benefit from Thermo Fisher Scientific services.
Meet The Experts: Part 2 - Raman Spectroscopy
Watch part 2 of this 4-part interview series to explore Raman spectroscopy, one of the main PAT tools for monitoring bioprocess CQAs and CPPs, with expert Fabien Caron.
How To Develop An Efficient Downstream Purification Process For bsAbs
Bispecific antibodies (bsAbs) have gained increasing interest in recent years. Learn how to develop an efficient downstream purification process for a cancer immunotherapy bsAb.
Redefine Your Oligonucleotide Manufacturing
Streamline oligo production and scale confidently. Explore high-performing, purpose-built automated equipment designed to ensure safety, efficiency, and purity, from synthesis through concentration.
Transform Your Chromatography Processes With An Innovative Approach
Learn how to achieve better resin utilization, minimize disruption to existing methods, and align your strategy with unique process goals.
Technology To Overcome Absorption Hurdles And Solubility Limitations
For poorly soluble drugs, overcoming absorption hurdles can hinder development. Explore a solution that empowers researchers to overcome solubility limitations and accelerate drug development.
How To Maintain A Nuclease Free Environment During mRNA Production
mRNA are singled-stranded, and their chemistry makes them more susceptible to enzyme degradation than double-stranded DNA. Learn how to maintain a nuclease free environment during mRNA production and purification.
Solvent-Free, Fusion-Based Amorphic Dispersion Process
Discover a solvent-free, fusion-based process that leverages frictional and shear forces to rapidly convert crystalline drugs and polymers into amorphous solid dispersions (ASDs).
How mRNA Manufacturers Disrupt The Industry
Learn how biopharmaceutical companies can apply proven strategies to overcome hidden complexities in mRNA production, and discover solutions that can help you rapidly design and build a SU facility.
CESS Technology
Learn how the award-winning CESS® technology can be used in Nanoforming™ future medicines to increase bioavailability for molecules with poor solubility.