Webcasts

***Live: Friday, November 20, 2020 at 11am EST| 8am PST| 4pm GMT| 5pm CET*** Lipid multiarticulate (LMPs) are versatile drug delivery systems which offer flexibility in both drug release and final dosage form. This webinar discusses the process for formulation selection and LMP manufacturing through the lens of visual techniques.*** On demand available after final airing until Nov. 20, 2021.***

Do you have concerns about particulate matter entering your parenteral drug product? Register for the Oct. 20 webcast, “Using Quality Principles to Analyze and Quantify Particulate Matter in Parenteral Packaging”. This webcast is part of a series focusing on The Path to Patient Safety: Addressing Industry Concerns and Solutions for Primary Packaging Component Selection. Live: Part III: Tuesday, Oct. 20, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after airing until Oct. 20, 2021 Register free

***Live: Monday, Oct. 19, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST*** Learn about the challenges of N-nitrosamines analysis and mass spectrometry and complimentary orthogonal mass spectrometry techniques can be used to address these challenges.. *** On demand available after final airing until Oct. 19, 2021.***

***Live: Wednesday, November 4, 2020 at 11am EST| 8am PST| 4pm GMT| 5pm CET ***Looking for best approach to control the critical quality attributes of your API? Hear experts from Janssen and WuXi STA describe current technologies in API crystallization and their experience in building robust processes.***On demand available after airing until Nov. 4, 2021

***Live: Wednesday, November 18, 2020 at 10am EST | 9am CST | 3pm GMT | 4pm CET *** Scientific leaders from the United States Pharmacopoeia (USP) and Biogen share perspectives on addressing challenges in chemistry, manufacturing, and controls testing, and provide insights and strategies for a successful path from drug development to commercial manufacturing.***On demand available after airing until Nov. 18, 2021

*** Live: Thursday, November 5, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET***At the center of every clinical trial is a patient awaiting treatment. Learn from the experts on how to design a decentralized clinical trial to improve patient recruitment and retention. ***On demand available after final airing until Nov. 5, 2021***

*** Live: Thursday, October 22, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST*** Be sure you’re using the latest XRD sample preparation and measurement strategies while confidently meeting audit trail and compliance requirements. Learn how recent software solutions enable straightforward, compliant pharmaceutical workflows. ***On demand available after final airing until Oct. 22, 2021***

*** Live: Monday, Oct. 26, 2020, 11am EDT| 8am PDT| 3pm GMT| 4pm CET *** What are typical challenges sponsors encounter during Phase 3 clinical trials? How can advance preparation during Phase 2 help mitigate risks? Learn effective strategies to avoid surprises and problems in late-stage trials from experience clinical trial and supply experts. ***On demand available after final airing until Oct. 26, 2021***

*** Live: Thursday, Oct. 15, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST *** Polymorph screening of small-molecule drug candidates enables rational selection of the proper solid form/polymorph for further development. Learn the elements and techniques of polymorph screening is and why performing it thoroughly will help de-risk drug development effort. ***On demand available after final airing until Oct. 15, 2021***

***Live: Wednesday, Oct. 21, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST*** Non-destructive moisture determination of freeze-dried product saves valuable samples and enables efficient robust data generation supporting lyophilization cycle development and freeze-dryer qualification activities. Join this webcast to hear case study data demonstrating these applications. ***On demand available after final airing until Oct. 21, 2021***

In this webcast, Michael Grass PhD (Head of Solid Form Services, Global R&D) will present how solid form screening is performed and the importance of this work to drug substance and drug product development. Live: Thursday, Sep. 10, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Sep 10, 2021 Register free

Learn how to navigate the regulatory requirements for extractables and leachables testing for new biologic drug products. Review the essential steps to for study design, extraction, analysis, and reporting of extractables and leachables data in this webcast. Live: Thursday, Sept. 24, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing until Sept. 24, 2021

In this webcast, Brett Lane, Senior Chemist of Lonza’s QC laboratory in Rochester, NY will share his experience modifying titration manual methods to optimize results using autotitration. Live: Wednesday, Sept. 23, 2020 at 1pm EDT | 12pm CDT | 10am PDT On demand available after final airing until Sept. 23, 2021

Would you like to learn more about the E&L qualification process of the primary packaging for lyophilized drug products? Then make sure to attend this 45-minute webinar, given by Piet Christiaens scientific director at Nelson Labs Europe. Live: Thursday, Oct. 15, 2020 at 2pm EDT| 1pm CDT| 11am PDT On demand available after final airing until Oct. 15, 2021

Stability and moisture challenges are likely to increase with the development of more potent APIs, larger molecules, and modified-release tablets. Learn about innovative packaging solutions to address the increasing need to protect hydrophilic oral solid doses from moisture and preserve drug stability. Live: Thursday, Sept. 17, 2020 at 11am EDT| 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Sept. 17, 2021

Review how data-driven approaches, including physiologically based pharmacokinetic (PBPK) modeling, parallel formulation screening, API sparing techniques, and optimal early dosing strategies can help avoid development pitfalls for small-molecule drug candidates on the path to clinic. Live: Wednesday, Sept. 23, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after final airing until Sept. 23, 2021

Listen and learn as Dr. James Grinias from Rowan University and Dr. Frank Steiner from Thermo Fisher Scientific discuss approaches and considerations to modernizing HPLC methods to increase throughput using superficially porous particles. They also discuss challenges in method transfer and describe new compliant hardware technologies built into the modern HPLC and UHPLC systems. Live: Tuesday, Aug. 25, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing until Aug. 25, 2021

The promises of the digital lab are enticing but getting there can seem daunting. The good news is that you can start today. It’s simply about implementation, and not waiting for innovation. Live: Tuesday, Sept. 22, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after airing until Sept. 22, 2021

Learn about the use of molecular spectroscopy techniques – transmission Raman spectroscopy (TRS) and laser direct infrared (LDIR) – for solid-state analysis in pharmaceutical formulation development. Live: US & Europe: Tuesday Sept. 29, 2020 at 9am EDT | 2pm BST | 3pm CEST, US: Tuesday Sept. 29, 2020 at 4pm EDT | 3pm CDT | 1pm PDT, Asia Pacific: Wednesday, Sept. 30, 2020 at 10:30am IST | 1pm CST | 2pm JST | 3pm AEST On demand available after airing until Sept. 30, 2021

This webinar will describe raw material verification testing through transparent and non-transparent packaging using the new Agilent Vaya handheld Raman system. True through-barrier analysis removes the need for sampling, increasing testing throughput without increasing costs—from clear glass vials to multilayer paper sacks. Live: US & Europe Broadcast: Thursday, Oct.1, 2020 at 9am EDT| 2pm BST| 3pm CEST, US Broadcast: Thursday, Oct. 1, 2020 at 4pm EDT | 3pm CDT| 1pm PDT, Asia Pacific: Friday, Oct. 2, 2020 at 10:30am IST| 1pm CST| 2pm JST| 3pm AEST On demand available after airing until Oct. 2, 2021

Near infrared (NIR) spectroscopy to the rescue: See how this vital process analytical technology tool can improve efficiency and cut costs in your pharmaceutical QC processes. Live: Wednesday, Sept. 9, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Sept. 9, 2021

What are the reasons for functional film coating of solid oral dosage forms? How do polymers influence the release of active ingredients in a tablet coating? Abderraouf Allia uses many practical examples and different formulations to show what needs to be taken into account during formulation. Participate in this webcast and learn how ready-to-use film coating systems can simplify the coating and formulation process. Live: Wednesday, Sept. 16, 2020 at 10 am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after airing until Sept. 16, 2021

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

The molecular complexity, size, and higher-order structure of gene therapies create a unique challenge for pharmaceutical development. This webcast will provide insights into characterizing viral and non-viral gene therapies to ensure quality. Live: Thursday, Aug. 20, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Aug. 20, 2021

This webcast focuses on manufacturing aspects of amorphous spray-dried dispersions to enable successful scale-up and optimization of the process. An overview of spray drying and typical scale-up challenges will be presented along with a robust process development strategy to ensure critical-to-quality attributes are maintained. Tools and methodologies that enable rapid scale-up that is right the first time from clinical to commercial scale will also be highlighted. Live: Tuesday, Aug. 4, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Aug. 4, 2021 Register free

If you have a new compound for respiratory drug delivery, what particle engineering approach should you take? This webinar will explore both micronization and spray drying approaches in relation to product performance of the inhaled drug product. Live: Thursday, Jul. 30, 2020 at 11am EDT | 8am PDT | 4pm GMT | 5pm CEST On demand available after airing until Jul. 30, 2021 Register free

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