Webcasts
The Ever-Changing World of Extractables and Leachables
August 12th 2020Join 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
Analytical Tools for PAT Implementation for the Characterization of Biosimilars
July 30th 2020This 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
Editors’ Series: Cell and Gene Therapies: Laying the Foundation for a New Supply Chain
July 29th 2020Existing 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
Editors’ Series: Overcoming Commercialization Challenges for Cell Therapies and Gene Therapies
July 28th 2020The 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
Validation of LC-MS Multi-Attribute Method (MAM) Supporting Biopharma Process Characterization
June 30th 2020An 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
Accurate Weighing of Reference Standards in a QC Laboratory
May 28th 2020For 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
Viral Vector Process Development: Applying CE and MS Techniques for In-Process Testing
May 27th 2020Fast growth in cell and gene therapy industry has generated an urgent need for fast and robust analytics for characterization and impurity determination for viral vectors. Mass spectrometry (MS) and capillary electrophoresis (CE) open up new avenues to enable fast and actionable analytics to enable quicker development and commercialization of gene therapies. Live: Wednesday, May 27, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing until May 27, 2021
Implementing Attribute Monitoring Analyses for Biopharmaceutical Development and QC
April 29th 2020Join 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
Ensuring the Continuous Supply of Quality Drug Products During Uncertain Times
April 28th 2020The 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
An In-Depth Look at Intact Biotherapeutic Characterization and Quantitation in Biological Matrices
April 23rd 2020This 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
Multi-Level Workflows for Quantitative N-Glycan and Sialic Acid Analysis of Biotherapeutics
March 31st 2020Working 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
Thorough and Reproducible Analytical Characterization of Innovator and Biosimilar Pair
December 11th 2019In 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
Access Monoclonal Antibody Quality Attributes with HRMS Analytical Power
December 5th 2019In 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
Platform Purification Approaches for the Production of Complex Biologics
December 4th 2019In 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
Advancing mAb Charge Variant Characterization Using Native, On-Line IEX-MS Technology
December 4th 2019Learn 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
Assays to Evaluate Fragment Crystallizable (Fc)-Mediated Effector Function
November 1st 2019This 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
Choosing The Right CDMO For Late-Phase Clinical Trials
October 30th 2019For many pharmaceutical companies that do not have their own facilities, choosing the right partner for late-phase clinical trials and commercial production is a critical aspect in the management of parenteral products. Join Christy Eatmon, Global SME, Sterile Drug Products at Thermo Fisher Scientific, where she will lead a webcast that will offer insight into the importance of looking for a partner with extensive experience in the parenteral arena. Live: Wednesday, Oct. 30, 2019 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after final airing Oct. 30, 2020 Register free
