Webcasts

*** 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: Tuesday, Oct. 27, 2020 *** Multi-layer tableting offers an inexpensive and straightforward solution for a variety of challenging formulations. Learn how multi-layer formulations compare to traditional methods, gain insight to the multi-layer tableting process, and crucial tips to formulating and manufacturing robust multi-layer tablets. ***On demand available after final airing until Oct. 27, 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