Broadcast 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
Wednesday, 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.
**Wednesday, November 10, 2021 at 11am EST| 8am PST| 4pm GMT| 5pm CET** Unfold the power of oligonucleotide purification using a hydrophobic interaction resin in one-step chromatography method.
**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.
Wednesday, 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.
October 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.
Wednesday, 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.
Thursday, 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.
Tuesday, 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.
Thursday, 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.
Wednesday, 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.
Thursday 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.
Thursday, 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.
Tuesday, 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.
Thursday July 22, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST Learn how to detect replication competent virus in your gene therapy and what regulators are looking for when testing viral vectors.
Tuesday, July 20, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST With changes and updates happening in drug development, learn about challenges associated with new modalities, FDA updates, and resource shortages.
Thursday, 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.
Wednesday, July 14, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST
Tuesday, 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.
Wednesday, July 7, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
Wednesday, June 30, 2021 at 2:30-6:30pm CEST | 8:30am-12:30pm EDT Session 1: 2:30-4:30pm CEST | 8:30-10:30am EDT Session 2: 4:30-6:30pm CEST | 10:30-12:30pm EDT
Wednesday, June 23, 2021 at 10am EDT| 7am PDT| 3pm BST| 4pm CEST
Friday, June 11, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
*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*
*Wednesday, May 26, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST* Unfolding the power of mAb purification via N-linked glycans using a FcR-IIIA resin and how it compares to protein A resin. *On Demand Until May 26, 2022*
*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*
***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***
*Wednesday, May 19, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST* The selection of single-use materials for novel gene therapies, as well as the material’s commercial viability, is crucial especially for those used in storage and cryogenic operations. Learn about key product contact material and process compatibility requirements during this webcast. *On Demand Until May 19, 2022*
*Europe Broadcast: Tuesday, May 18, 2021 9am EDT | 2pm BST | 3pm CEST and US Broadcast: Tuesday, May 18, 2021 2pm EDT | 1pm CDT | 11am PDT* Biopharmaceutical companies are transitioning from “quality-by-testing” philosophy to “quality-by-design” paradigms, and establishing QbD-based PAT tools to increase product and process understanding. Due to the deficit of analytical methods to support QbD-driven continuous bioprocessing, biopharmaceutical companies are actively developing PAT tools to comply with QbD regulations. *On Demand Until May 18, 2022*
*Tuesday, May 11, 2021 at 9am EDT | 2pm BST | 3pm CEST, Tuesday, May 11, 2021 at 2pm EDT | 1pm CDT | 11am PDT* Adeno-associated viruses (AAVs) are an important tool enabling the delivery of next-generation gene therapies. *Available On Demand Until May 11, 2022*
