Webcasts
Rapid Analysis of mRNA 5’ Capping and Poly-A Tailing with High-Resolution LC-MS
January 11th 2022Tuesday, January, 11th, 2022 at 9am EST | 3pm CET | 2pm GMT Tuesday, January, 11th, 2022 at 2pm EST | 11am PST | 7pm GMToin us in our expert discussion of Rapid Analysis of mRNA 5’ Capping and Poly-A Tailing with High-Resolution LC-MS. See how mRNA capping can be analyzed by LC-MS within 75 minutes!
Novel approach to automating Maxi-, Mega-, and Giga-plasmid DNA preparations
December 2nd 2021Broadcast 1 (APAC): Thursday December 2, 2021 at 10:00am CST | 11:00am JST Broadcast 2 (EMEA): Thursday December 2, 2021 at 2:00pm GMT | 1:00pm CET Broadcast 3 (Americas): Thursday December 2, 2021 at 2pm EST | 1pm CST | 11am PST Interested in automating your plasmid purification work? Learn how you can automate your Maxi, Mega and Giga preparations with consistent purity and transfection efficiency
Automating Routine Analysis of Therapeutic mAbs in High Volume Applications
December 1st 2021Wednesday, December 1st, 2021 at 11 am EST | 10 am CST | 8 am PST Learn how to accelerate therapeutic mAbs workflows by automating analysis of critical quality attributes (CQAs) such as Fc glycosylation, oxidation, C-terminal lysine clipping, and glycation.
Impact of Scalable Freeze/Thaw Cycling on Protein Stability & Structure
October 27th 2021**Wednesday, October 27, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST** Freezing and thawing at scale of API and BDS biologics is not routine and should be handled with the consideration given to any critical unit operation. This webinar highlights key protein related quality challenges associated with freeze methods. Optimization thorough model freeze/thaw studies are presented.
Moving SWATH LC–MS Host Cell Protein Analysis into a GMP Environment?
October 6th 2021Wednesday, October 6, 2021 at 12pm EDT | 9am PDT | 5pm BST | 6pm CEST In this webinar, you will learn about the possibility of GMP method transfer for HCP assays leveraging a robust and automated workflow based on combining data-dependent and data-independent mass spectrometry. A study of data from multiple projects over three years demonstrated the robustness and reproducibility of the method.
The Ever-Changing World of Extractables and Leachables: Lessons learned and future challenges
October 4th 2021October 4, 2021 at 3pm BST | 10am EST | 4pm CEST Join global industry and regulatory experts as they discuss current hot topics in extractables and leachables (E&L) testing for pharmaceuticals, biopharmaceuticals and medical devices.
Increasing Upstream Bioprocessing Efficiency through Process Analytical Technology
September 29th 2021Wednesday, September 29, 2021 at 10am EDT| 7am PDT| 3pm BST| 4pm CEST Learn about strategies for inline process analytics aimed at automated feed control in an upstream bioprocess. Using the example of a Raman analyzer, a glucose analyzer, and an exhaust analyzer experts demonstrate how to achieve seamless sensor integration with the bioprocess control software.
Personalized Medicines: Advances in Genetics and Bioinformatics
September 23rd 2021Thursday, September 23, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST Find out about the challenges of manufacturing personalized medicines and the lessons being learned from the pandemic with a vaccine developer and process equipment manufacturers.
Improve Ion Exchange Methods with Faster Method Development and Lower Dispersion
September 21st 2021Tuesday, September 21, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Want faster method development? Better ion exchange methods? Lower dispersion? Learn the latest techniques and innovations to optimize your applications and workflows.
Vector in HyPerforma Single-Use Bioreactors (S.U.B.s) using ExpiSf Expression System
September 16th 2021Thursday, September 16, 2021at 11am EDT| 8am PDT| 4pm BST| 5pm CEST Thermo Scientific HyPerforma Single Use Bioreactors (S.U.B.s) are widely used in the biopharma industry and can be used for a broad range of processes. With the rapid growth of the viral vector gene therapy industry, having a trusted partner is crucial to the success of scaling these processes. This webinar focuses on the scalability of both the HyPerforma 5:1 S.U.B. and the HyPeforma DynaDrive S.U.B. for growth and transfection of ExpiSf insect cells for adeno-associated virus vector production.
Technology Forum: The Next Steps for Pharma Manufacturing Efficiency and Effectiveness
September 15th 2021Wednesday, September 15, 2021 at 10am EDTDrug manufacturing demands and increased regulatory oversight are prompting pharmaceutical manufacturers to consider new processes for oral solid dose and aseptically processed drugs. A cross-section of industry experts will offer insight on emerging trends, technologies, and processes in this Technology Forum.
The Next Generation of Software Validation: Self-Validating Software
September 9th 2021Thursday September 9, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST Is computer software validation (CSV) holding you back from adopting the latest technology. Join this webinar for a look at the future of software validation and how it will remove the documentation burdens.
Method Robustness and Transferability for Modern Size-Exclusion Methods
August 26th 2021Thursday, August 26, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Developing a robust, transferable size-exclusion chromatography (SEC) method for routine testing of mabs and other biotherapeutics can be challenging. Join us for this presentation to learn about SEC method development, with an emphasis on method transfer and sustainability.
Analysis of Viral Proteins, Nucleic Acids and Biomolecular Interactions with Light Scattering
August 17th 2021Tuesday, August 17, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST Characterizing viral proteins and their interactions is key to understanding of how a virus infects cells and for the development of protein-based drugs. Learn how light scattering technology can be used for the biophysical characterization of viral proteins, mAbs, and their interactions.
Gene Therapy Manufacturing: A Dual Platform Reconciling Adherence and Suspension Approaches
July 15th 2021Thursday, July 15, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST What adherence and suspension-based technologies are best for gene therapy production? In this webinar, learn about a next-generation dual platform solution for viral vector manufacturing that helps to overcome existing barriers to scaling and commercializing gene therapies.
Dive Into Summer's Latest Innovations and Best Practices for Biopharma
July 13th 2021Tuesday, July 13, 2021 at 10am EDT | 3pm BST | 4pm CEST Biopharmaceuticals or biologics are a diverse class of compounds that need special attention from discovery, CQAs analysis, manufacturing and QC. Liquid Chromatography is an essential tool for structure characterization, PTM, glycan analysis and quality control of biopharmaceuticals. In this webinar, speakers will discuss the current challenges analytical laboratories face when manufacturing or analyzing biologics and how the hurdles of compromised sample integrity, process analytical integration, and surface interaction may be overcome. Whether analyzing large biomolecules, mAbs, intact proteins, oligonucleotides, aggregates, charge variants, ADCs, peptides, glycans or spent media, there is something for everyone.
Why Flexible End-to-End Solutions Succeed in BDS Handling
May 27th 2021*Thursday, May 27, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST* Transportation of your bulk drug substance (BDS) from downstream to the fill/finish site might not be as simple as it sounds. Mostly geographically detached, each batch of BDS is filled into different primary packaging, frozen to sub-zero temperatures, stored, and shipped before it is then thawed and drained at the fill/finish site. *On Demand Until May 27, 2022*
Bridging the Digital Divide to Advance Bio/Pharma Manufacturing and Quality: A Technology Forum
May 25th 2021*Tuesday, May 25, 2021 at 10am EDT* The bio/pharma industry is turning to proven digital technologies used in other industries to plan, develop, and monitor manufacturing processes, as well as in quality, training, and regulatory oversight. In this event, experts discuss how artificial intelligence, remote monitoring, digital twins, and other technologies can be applied to modernize bio/pharma processes and systems. Lessons learned from the pandemic will be shared. *On Demand Until May 25, 2022*
Method Development Strategies for Purity Analysis of Proteins by Intact and Subunit Analysis
May 24th 2021***Live: Monday, May 24, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** Join us to learn best practices in method development for intact and subunit purity analysis for mAbs by reversed-phase liquid chromatography (RPLC), including how to best adjust method parameters such as temperature, gradient slope, and flow rate to obtain high-quality impurity profiling and ensure method robustness and reproducibility. ***On Demand until May 24, 2022***
