Webcasts

Join global industry and regulatory experts as they discuss current E&L hot topics on pharmaceuticals, biopharmaceuticals and medical devices. Live: Wednesday, Sept. 9, 2020 at 9am EDT | 2pm BST | 3pm CEST On demand available after final airing until Sept. 9, 2021

Join us for this webcast, in which Zuzana Demianova will present the analysis of low abundant mannose glycopeptides of adalimumab along with a highly sensitive peptide mapping analysis of adalimumab. Live: Wednesday, Aug. 26, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing until Aug. 26, 2021

This event will aim to present an overview of how analytical technologies can be adapted for implementation of Process Analytical Technology (PAT) in bioprocessing and how this can result in effective process control, thereby delivering consistent process performance and product quality. Live: Europe Broadcast: Thursday, Jul. 30, 2020 at 9am EDT| 2pm BST| 3pm CEST US Broadcast: Thursday, Jul. 30, 2020 at 2pm EDT| 1pm CDT| 11am PDT On demand available after final airing until Jul. 30, 2021

Existing biopharma supply chain practices must evolve to meet the needs of personalized therapies, particularly for autologous treatments. Force fitting manual processes will no longer work. Hear about lessons learned in a pioneering “vein to vein” pilot program that aims to establish new rules for data management and exchange, scheduling, and automating workflow and supply chain practices for novel and complex processes. Live: Wednesday, Jul. 29, 2020, at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On Demand: available after airing until Jul. 29, 2021 Register free

The complexities of producing cell therapies and gene therapies are testing established biomanufacturing practices and the companies engaged in producing the treatment. Join this webcast to hear about the technical and regulatory hurdles associated with development and manufacturing steps, and strategies and solutions to facilitate development through commercialization. Live: Tuesday, Jul. 28, 2020, at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On Demand: available after airing until Jul. 28, 2021 Register free

The discovery of nitrosamine-based impurities in APIs has triggered recalls of commonly used drugs and placed the quality of the drug supply in question. Learn best practices for identifying impurities in drug substances and drug products and the roles and responsibilities of ingredients suppliers, drug manufacturers, and regulatory authorities. Live:Tuesday, Jul. 14, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On Demand: available after airing until Jul. 14, 2021 Register free

An automated multi-attribute method (MAM) approach providing high-throughput, user-friendly analysis of process validation samples is moving mass spectrometry toward biopharma quality control. Learn how to implement automated MAM approaches for process development and validation and streamline approaches using a single scalable enterprise software platform. Live: Tuesday, Jun. 30, 2020 at 10am EDT | 9am CDT | 2pm BST | 3pm CEST On demand available after final airing Jun. 30, 2021 Register free

How can you better identify those host cell proteins (HCPs) that might co-purify with your drug substance (DS) and elicit an undesired immune response, interfere with drug safety and efficacy, or impact DS stability? Cygnus Technologies VP of R&D, Eric Bishop, will discuss powerful orthogonal methods such as immunoaffinity chromatography and mass spectrometry that enable full understanding of those HCPs that are present in the product and could potentially impact patient safety and drug stability. Live: Tuesday, Jun. 16, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after airing until Jun. 16, 2021 Register free

For any quantitative HPLC experiment, the accurate preparation of verified standards is necessary and reliant on accurate weighing procedures. Learn about practices to ensure accurate measurements in quality control laboratories. Live: Thursday, May 28, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after airing until May 28, 2021 Register free

Learn how to achieve better resolution, reproducibility, and quality data for intact mAb and sub-unit analysis. In this webcast, Brian Rivera will review method optimization for a new wide pore C4 core-shell particle that further exhibits improved efficiency and robust separation for large molecules. Live: Thursday, May 21, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing May 21, 2021 Register free

Join Ankita Desai from Eppendorf and Arie Reijerkerk from Ncardia in this webcast and Q&A session to learn about the benefits of stirred-tank bioreactors for the drug discovery and development process. Get insights about how the advent of human-induced pluripotent stem cell (hiPSC) technology has substantially expanded the availability of human cells. On demand available until May 21, 2021 Register free

Learn about vaccine biophysical characterization, PAT, and QC using light scattering technologies. Live: Tuesday, May 19, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 19, 2021 Register free

This PharmaTalks session focuses on how the integration of Patheon into Thermo Fisher Scientific has resulted in unique opportunities for innovation, collaboration, and technology development, and how we are leveraging the Thermo Fisher ecosystem to develop and improve a platform for biopharmaceutical manufacturing Available On Demand Register free

Are you seeing the whole picture with your current analysis tools? Join us to learn how low volume, high throughput particle analysis with BMI provides more information and faster insights at any stage of biologic development – even at high concentrations. Live: Tuesday, May 12, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 12, 2021 Register free

Join us for a free webcast on April 29th to learn about the advantages of using high-performance LC-MS and how you can obtain quality results. In this webcast will cover the latest developments in the use of high-performance LC-MS for biopharmaceutical analysis, including transitioning product characterization knowledge into monitoring assays for product and process related quality attributes of biopharmaceuticals. Live: Tuesday, April 14, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing until April 14, 2021

The global coronavirus pandemic has tested the abilities of bio/pharmaceutical companies to develop new therapies and maintain-or even accelerate-production of existing drugs. In this webcast, experts will discuss business continuity practices, regulatory compliance, and supply chain management under current-or future-emergency conditions. Live: Tuesday, Apr. 28, 2020 at 11 am EDT | 10 am CDT | 8 am PDT On Demand: available after airing until Apr. 28, 2021 Register free

This webcast discusses a highly sensitive and automated workflow for intact biotherapeutic characterization and quantitation from biological matrices. We will also discuss native protein characterization and its challenges. Europe Broadcast: Thursday, Apr. 23, 2020 at 9am EDT | 2pm BST | 3pm CEST US Broadcast: Thursday, Apr. 23, 2020 at 2pm EDT | 1pm CDT | 11am PDT On demand available after final airing until Apr. 23, 2021

Working with glycosylated therapeutics? Join Aled Jones and David Wong for a discussion of multi-level LC/FLD/MS quantitation workflows for N-glycan analysis of biotherapeutics, including intact mass, subunit, glycopeptide, released glycan, and sialic acid monosaccharide analysis. Tune in to learn about how these options can help you. Live: Europe & US Broadcast: Tuesday, Mar. 31, 2020 at 9am EDT | 2pm BST |3pm CEST US Broadcast: Tuesday, Mar. 31, 2020 at 2pm EDT | 1pm CDT | 11am PDT Asia Pacific: Wednesday, Apr. 1, 2020 at 8:30am IST | 12pm JST | 2pm AEDT On demand available after final airing Mar. 31, 2021 Register free

Oligonucleotides are a chemically distinct class from small-molecule or protein therapeutics and present their own unique challenges for characterization and quantification. In this webcast you will learn how high-resolution mass spectrometry (HRMS) and microflow LC-MS can help you overcome these challenges and still maintain a high level of sensitivity. Live: Tuesday, March 17, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after final airing until Mar. 17,, 2021 Register free

Review best practices for measurement of trace elements in cell culture media and hydrolysates, developed in a collaboration between USP and the BioPhorum Operations Group. Live: Tuesday, Mar. 3, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET On demand available after airing until Mar. 3, 2021 Register free

Learn about real-time light scattering, a novel technology for measuring quality attributes of bio- and nano-pharmaceuticals directly in the process stream. Live: Wednesday, Feb. 26, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET On demand available after airing until Feb. 26, 2021 Register free

In this webcast we will present Agilent samples to answers workflow solutions for monoclonal antibody characterization. The presentation covers analytical strategies for monitoring CQAs. We will focus on main quality attributes such as charge variants, aggregation, glycosylation, host cell protein impurities and post-translational modifications. Live: Europe: Wednesday, Feb. 5, 2020 at 2pm GMT | 3pm CET US: Wednesday, Feb. 5, 2020 at 2pm EST | 1pm CST | 11am PST On demand available after final airing until Feb. 5, 2021 Register free

In this webcast, use of advanced analytical techniques to thoroughly characterize and compare biosimilar versions to innovator drug will be presented. Live: Europe Broadcast: Wednesday, Dec. 11, 2019 at 2pm GMT | 3pm CET North America Broadcast: Wednesday Dec. 11, 2019 at 2pm EST| 1pm CST | 11am PST Asia Pacific: Available On-Demand on Dec. 12, 2020 Register free

In the webcast, learn how using a high-resolution mass spectrometry-based approach can be a powerful analytical strategy to monitor and define multiple critical quality attributes (multi-attribute monitoring) of complex biomolecules in a single assay using a single instrument platform. Live: Thursday, Dec. 5, 2019 at 11am EST | 8am PST | 4pm GMT | 5pm CET On demand available after final airing until Dec. 5, 2020 Register free

In this webcast you will learn how next-generation IEX and HIC resins are able to address purification challenges of complex biologics, thereby improving product purity and recovery. In addition, you will see how these innovative purification solutions allow for high performance at faster flow rates, helping to increase throughput and process flexibility and ultimately realizing a more productive processes. Live: Wednesday, Dec. 4, 2019 at 8:30am IST | 11am CST | 12pm KST | 2pm AEDT On demand available after final airing Dec. 4, 2020 Register free

Learn tips for efficient analyses of mAb charge variants, at both the intact and subunit level, using ion-exchange chromatography (IEX) and detection via mass spectrometry (MS). Gain insight on tools and tactics for accurate quantitation and cleaner spectra with less undesired adduct noise or super charging. Live: Wednesday, Dec. 4, 2019 11am EST | 8am PST | 4pm GMT | 5pm CST On demand available after airing until Sept. 10, 2020 Register free

Dr. Grabski discusses why MCC offers significant economic advantages over traditional batch chromatography methods for purification of monoclonal antibodies. Live: Tuesday, Nov. 19, 2019 at 11am EST | 8am PST | 4pm GMT | 5pm CET Register free

This webcast will focus on industry best practices to develop and validate cell-based and non-cell-based formats for measuring Fc-mediated effector function activity including advantages, disadvantages, and points to consider for each assay format.. Live: Friday, Nov. 1, 2019 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after airing until Nov. 1, 2020 Register free