Webcasts

*Live: Wednesday, June 23, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST* Would you like to reduce development costs and accelerate time to market? Learn how to leverage virtual formulation assistants to predict tabletability and ingredient incompatibilities while considering the impact of material properties. *On Demand Until June 23, 2022*

*Tuesday, June 22, 2021 10am EDT| 7am PDT| 3pm BST| 4pm CEST* Over the past few years, the use of drug delivery devices has steadily increased, leading to a higher demand for cartridges. This webcast will introduce the audience to packaging components for cartridges used in drug delivery devices today and explore future trends that are emerging in the market. *On Demand Until June 22, 2022*

*Live: Tuesday, June 15, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST* With defined criteria for conductivity, total organic carbon, and bacteria, purified water is a critical ingredient and processing aid for many pharmaceutical companies. Learn how your facility can achieve consistent high purity quality water while reducing total maintenance and operating costs. *On Demand Until June 15, 2022*

*Two Live Airings: Wednesday, June 9, 2021 at 9am EDT| 3pm GMT & Wednesday, June 9, 2021 at 12pm EDT| 9am PDT* Join us for a hybrid/virtual event to celebrate the opening of PPD Laboratories’ newest lab in Suzhou, China. Hear from PPD Laboratories leaders, take a virtual tour, and participate in a live Q&A. *On Demand Until June 9, 2022*

*Live: Thursday, May 27, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST* Compendial verification is a regulatory requirement. Often overlooked are the technical merits of a robust review of the written method and the value of demonstrating fit for purpose in your laboratory. Experts will share experiences gained over years of evaluating hundreds of methods to help you avoid similar obstacles and delays in your laboratory. *On Demand Until May 27, 2022*

*Tuesday, May 25, 2021 at 10am EDT* The bio/pharma industry is turning to proven digital technologies used in other industries to plan, develop, and monitor manufacturing processes, as well as in quality, training, and regulatory oversight. In this event, experts discuss how artificial intelligence, remote monitoring, digital twins, and other technologies can be applied to modernize bio/pharma processes and systems. Lessons learned from the pandemic will be shared. *On Demand Until May 25, 2022*

***Thursday, May 20, 2021, 2pm EDT | 1pm CDT | 11am PDT*** Flexible bag systems used for large-volume parenteral drug applications contain different materials that pose potential sources of contamination. In this webcast, learn about the sources of extractables and leachable, testing programs, regulatory requirements, and challenges specific to large-volume parenteral applications. *** On demand available after final airing until May 20, 2022.***

*Wednesday, May 19, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST* Listen and learn as Alexander Schwenger from CureVac and Frank Steiner from Thermo Fisher Scientific discuss the highlights of 2-dimensional LC and innovative use cases and discuss current and future challenges in in vaccine research, development, and production. *Available On Demand May 19, 2022*

Two Airings! * NA, EMEA, LATAM: Tuesday, May 18, 2021 at 11am EDT |8am PDT| 4pm BST| 5pm CEST and APAC: Tuesday, May 25, 2021 at 4pm JST| 3pm CST| 5pm AEST| 12:30pm IST* Learn more about possible solutions to help overcome the challenges of formulating poorly absorbable APIs with different oral dosage forms. *On Demand Until May 25, 2022*

*Thursday, May 6, 2021 at 2pm EDT | 1pm CDT | 11am PDT* Learn how artificial intelligence can be used to investigate corrective and preventive actions, pinpoint the root cause of the most common complaints, tell if training is effective, and identify the combination of materials and workers to increase production. *On Demand Until May 6, 2022*

*Wednesday, May 5, 2021 at 10am EDT | 7am PDT | 3pm BST | 4pm CEST* What size API would work for an ODT targeting sublingual or enteric delivery? Why would one consider an ODT over a tablet or capsule for standard G.I. absorption? Learn more as Catalent discusses ODT technologies in this upcoming webinar. *On Demand Until May 5, 2022*

*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 <922> “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.***

***Live: Wednesday, February 24, 2021, 1pm EST | 10am PST | 6pm GMT | 7pm CET*** Titration plays an important role in pharmaceutical analysis. Despite the recent attention given to chromatographic methods, several applications are only feasible by titration, making it a fit-for-purpose method for many analytes. For example, distinguishing between carbonate and bicarbonate or monobasic and dibasic phosphate salts can only be accomplished by titration. *** On demand available after final airing until Feb. 24, 2022.***

***Live: Wednesday, February 24, 2021 at 10am EST | 3pm GMT | 4pm CET*** Join global industry and regulatory experts as they discuss current E&L hot topics related to pharmaceuticals, biopharmaceuticals and medical devices. ***On demand available after final airing until Feb. 24, 2022***

***Live: Tuesday, February 23, 2021, 11am EST | 8am PST | 4pm GMT | 5pm CET*** The combination of Quality 4.0 and a global pandemic created a pressing need for organizations to automate quality and compliance processes by deployment a digital quality management system. Learn about the technologies that are creating a paradigm shift within the quality and compliance space and common pitfalls to avoid when automating quality and compliance processes.*** On demand available after final airing until Feb. 23, 2022.***

***Live: Thursday, January 28, 2021 at 11am EST | 8am PST | 4pm GMT | 5pm CET*** Amorphous solid dispersions (ASDs) are a critical technology for bioavailability enhancement. In this webcast Lonza’s Deanna Mudie and Aaron Stewart discuss Lonza’s best practices for ASD formulation development and in vitro testing.*** On demand available after final airing until Jan. 28, 2022.***

***Live: Tuesday, January 19, 2021, at 11am EST | 8am PST | 4pm GMT | 5pm CET ***Join this webcast to learn best practices to ensure a smooth transition from Phase 1 to Phase 2 studies, how a clinical supply provider can enable this process, as well as the role that integrated solutions can play***On demand available after final airing until Jan. 19, 2022***

*** Available On Demand *** The aim of this presentation is to highlight the effect of various formulation components on the raft properties. ***On demand available after final airing until Dec. 21, 2021***

***December 8, 2020 at 10am EST| 3pm GMT| 4pm CET*** Join this live webcast to learn more about a unique and powerful integration between lab scheduling and lab procedure execution, leading to an 80% reduction in time spent planning and organizing work as well as 10x reduction in compliance risk through standardized processes..*** On demand available after final airing until Dec. 8, 2021.***

***Live: Wednesday, December 2, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET***Learn more about the recent trends in single-use sensors to match bioprocessing needs of bioreactor, fermenters, and mixing applications. Review data from 2-year studies of sensor testing.***On demand available after final airing until Dec. 2, 2021***

***Live: Tuesday, December 1, 2020 at 10am EST| 9am CST| 3pm GMT| 4pm CET***Formulators face special challenges with developing parenteral drugs to achieve the needed stability, efficacy and sterility. Learn how high purity excipients can be used to address formulation issues, while complying with regulatory requirements.*** On demand available after final airing until Dec. 1, 2021.***