Webcasts

*Thursday April 29, 2021 at 2pm EDT | 1pm CDT | 11am PDT* Interested in achieving an efficient and automated seed train in upstream processing? Do you have challenges in high cell density clarification using traditional hybrid approaches? Register now to find out how to overcome these challenges by applying process intensification, advanced process analytical technology and single-use centrifugation.

***Wednesday, April 28, 2021, 8AM PDT | 11AM EDT | 4PM BST | 5PM CEST*** This webinar brings together experts from LGC and PerkinElmer to share their perspectives on addressing challenges in excipients testing, as well as providing insights and strategies for a successful path for the control of impurities in excipients to achieve 21 CFR Part 11 compliance.*** On demand available after final airing until April 28, 2022.***

***Session 1: Thursday, April 22, 2021, 10am EDT, Session 2: Thursday, April 22, 2021, 11am EDT, Session 3: Thursday, April 22, 2021, 1pm EDT*** A drug’s journey from development to manufacturing to patients is paved with roadblocks and potholes; many threats can derail bio/pharmaceutical processes. Potential solutions to such pitfalls have been discussed for years; however, few manufacturers have embraced technology and process advances to proactively ensure drug supply chain continuity.

***Wednesday, March 31, 2021, 11am EDT | 8am PDT | 3pm CEST | 4pm BST*** The COVID-19 pandemic has highlighted the importance of being prepared, planning ahead, and diversifying resources to assure continuity of manufacture and supply of life-sustaining medicines. Learn about best practices to anticipate, manage, and overcome unexpected challenges to drug production during a global emergency. *** On demand available after final airing until March 31, 2022.***

***Now Available!*** Thinking about changing QC testing methods? Join Charles River’s Alan Hoffmeister for The Art of Changing QC Testing Processes to learn why saying yes to change can benefit you in the long run. *** On demand until March 30, 2022.***

***Live: Tuesday, March 30, 2021, 2pm EDT | 11am PDT | 7pm BST | 8pm CEST*** Join Dr. Tony Cundell, a member of the USP Expert Committee that crafted the new USP General Chapter “Water Activity,”¬¬¬ as he breaks down the implications of the new chapter and explains the role of water activity measurements in developing and producing drug products. Bring your questions for the live Q&A session afterward. *** On demand available after final airing until March 30, 2022.***

***Live: Thursday, March 25, 2021, 10am EDT| 7am PDT| 3pm GMT | 4pm CET*** For vaccine developers, the COVID-19 pandemic has posed challenges for packaging and distributing life-saving drug products. In this webcast, learn how parenteral packaging suppliers are ready to help vaccine developers overcome these challenges and prepare for future pandemic scenarios. *** On demand available after final airing until March 25, 2022.***

**Tuesday, March 23, 2021, 1pm EDT | 10am PDT | 6pm GMT | 7pm CET*** Biopharmaceutical products in development continue to increase in complexity, which poses a challenge for pharmaceutical companies that are looking to improve speed and efficiency of biologic development. Join us for this webinar where we will discuss new cell line development methodologies, as well as new instrumentation, that are enabling these complex programs to be performed with shortened development timelines. *** On demand available after final airing until March 23, 2022.***

***Live: Tuesday, March 9, 2021 at 11am EST | 8am PST | 4pm GMT | 5pm CET*** Review what needs to be put in place to ensure data integrity and compliance and minimize the risk for your organization. Learn how today´s state-of-the-art laboratory balance Cubis II from Sartorius provides all the technical features needed to automate processes to ensure pharma compliance and offers digital workflow support for trusted and error-free process. ** On demand available after final airing until March 9, 2022.***

***Live: Thursday, March 4 , 2021 at 11am EST| 8am PST| 4pm GMT| 5pm CET & Asia Pacific: Thursday, March 11, 2021 at 4pm JST | 3pm CST | 6pm AEST | 12:30pm IST*** Solid-form screening and characterization is a crucial part of drug substance development and pre-formulation. Review the underlying fundamentals of various screening methods and case studies on in-silico screening methods.*** On demand available after final airing until March 11, 2022.***