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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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Interested in learning more about the regulatory requirements for elastomeric components in parenteral drug packaging? Sign up for the July 22 webcast on “Best Practices for Meeting and Exceeding Regulatory Standards in Primary Packaging USP and ” . 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 II: Wednesday, Jul. 22, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after airing until Jul. 22, 2021 Register free
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Combining FTIR and Raman spectroscopy provides the insight needed to ensure appropriate distribution and concentration of APIs within tablets. Watch this webcast to learn more. Live: Tuesday, Jul. 21, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing Jul. 21, 2021 Register free
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Technology is more critical than ever to help you keep your clinical trials on track during the era of COVID-19. Gain best practices about how to empower your remote workforce, get critical regulated documents electronically signed compliantly, and to create a safe and flexible remote patient-centric experience. Live: Wednesday, Jul. 15, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Jul. 15, 2021. Register free
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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
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What is the correct approach for formulation development of poorly soluble NCEs? Dr. Umesh Barabde, director and operations head, Pharmaceutical Development Services, and Dr. Vishakh Kharat, director, analytical research, Pharmaceutical Development Services, both at Piramal Pharma Solutions discuss classic and specialized techniques to enhance solubility. Live: Thursday, Jun. 25, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing Jun. 25, 2021 Register free
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Dry powder inhalers (DPIs) are an important delivery technology for inhaled medicines in both respiratory and non-respiratory disease areas. Andreas Meliniotis, director of device development at Vectura, helps navigate the complex area of DPI product development and highlights the key considerations for both novel- and generic-drug programs. Live: Wednesday, Jun. 24, 2020 at 11am EDT |8am PDT |4pm BST |5pm CEST On demand available after final airing Jun. 24, 2021 Register free
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Want to be sure your systems and processes are compliant? Learn how two enable 21 CFR Part 11 in the lab with compliant workflows and consistent testing. Be confident in your analyses! Live: Tuesday, Jun. 23, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing Jun. 23, 2021 Register free
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This webinar will review Lonza’s integrated clinical supply services inclusive of manufacturing, primary and secondary packaging, kitting, and distribution with special emphasis on complex clinical studies and direct-to-patient shipping. Live: Tuesday, Jun. 23, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Jun. 23, 2021 Register free
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Recording and tracking data streams in real-time, within GMP facilities is challenging. Learn how voice-powered digital lab assistants provide a solution by directly communicating with lab instruments and by automatically transcribing voice notes from staff to ensure data can be attributed to staff members via user identification, automatic timestamps, and electronic signatures. Live: Monday, Jun. 22, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Jun. 22, 2021 Register free
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Preformulation studies play a significant role in developing approaches to analytical and formulation development based on the physicochemical properties of small-molecule pharmaceuticals. This webinar will provide insights into the preformulation phase of drug development and will illustrate common issues encountered. Live: Thursday, Jun. 18, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing Jun. 18, 2021 Register free
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When planning for commercialization for your product, your pharmaceutical packaging strategy is critical to the success of your project. Watch this webinar to learn how to build the right packaging strategy for your project based on product size and growth path. Live: Wednesday, Jun. 17, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after final airing Jun. 17, 2021 Register free
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When formulating a tablet, the solubility of the tablet matrix is often used as the sole criteria for disintegrant selection. Most formulators tend to select swelling-type disintegrants for insoluble matrices and wicking-type disintegrants for soluble matrices. This webcast will present an in-depth analysis of the effects of disintegration mechanisms, pH of test media, matrix plasticity, tablet hydrophobicity, and storage effects on the disintegration behavior. Live: Wednesday, Jun. 10, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Jun. 10, 2021 Register free
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This session of PharmaTalks focuses on the challenges of medication adherence in children and patients with swallowing disorders (dysphasia). On demand presentation Register free
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Self-emulsifying drug delivery systems, or SEDDS, are arguably the most successful technology in the market today for taking poorly water-soluble APIs and turning them into bioavailable formulations. But where do you start? Learn about the physical chemistry of these systems, discuss testing options, and uncover 10 ready-to-use formulations to be used for your next project. Live: Thursday June 4, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On Demand: available after airing until June 4, 2021 Register free
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Don’t just rely on packaging to protect drug products from moisture. In this webcast, discover how to develop more stable formulations by selecting the right excipients for use with moisture-sensitive drugs, and in doing so, reduce the risk of degradants and impurities. Live: Asia Pacific: Wednesday, Jun. 3, 2020 at 12pm IST | 2:30pm CST | 3:30pm JST US and Europe: Wednesday, Jun. 3, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after airing until Jun. 3, 2021 Register free
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Dominic Warrino and John Perkins of KCAS will provide an overview of recent developments in the pharmaceutical and bioanalytical industries outside of what is being done to address COVID-19. They will also examine case studies looking at the scientific challenges that KCAS continues to see on a daily basis. Live: Friday, May 29, 2020 at 11am EDT | 8am PDT | 4pm BS T| 5pm CEST On demand available after airing until May 29, 2020 Register free
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In this exclusive webcast, MasterControl’s Product Management Director Sue Marchant examines why document dependency has become a hindrance to manufacturers and how companies can successfully chart a clear path to digital and data maturity. She also explains the drivers behind the industry’s shift away from document-centered quality management and explores trends relating to digital quality management. Live: Thursday, May 28, 2020 at 2pm EDT| 1pm CDT| 11am PDT On demand available after airing until May 28, 2021 Register free
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Looking for the right approach to advance your small molecule drug candidate? Philip Jones from MD Anderson Cancer Center shares thoughts on how to bring drug candidates to Phase I clinical trials. Live: Wednesday, May 27, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 27, 2021 Register free
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Learn how biopharmaceutical development and production can be more efficient by using modular technology. Live: Wednesday, May 27, 2020 at 2pm EDT | 1pm CDT | 11am PDT On demand available after airing until May 27, 2021 Register free