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 <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.***

*** Live: Wednesday, November 11, 2020 | 8:30 AM EDT – 4:00 PM EDT *** 2020 Bio/Pharma Virtual Congress: Join Pharmaceutical Technology® and BioPharm International® for this online event that will explore the latest developments in formulation, manufacturing, and innovative drug dosage forms, as well as detailed discussions about crucial topics impacting the industry. ***On demand available after final airing until 11/11/2021

***Live: Tuesday, November 17, 2020 at 11am EDT| 8am PDT| 4pm GMT| 5pm CET***Oncology drugs dominate today’s industry pipeline, increasing the pressure on pharmaceutical scientists to get medications to patients as quickly as possible. But does the focus on speed mean sacrifices are made elsewhere in the development plan? Drug developers need to be mindful of the development challenges that come with oncology drug products in order to accelerate to proof-of-concept and onwards towards a successful commercial launch. *** On demand available after final airing until Nov. 17, 2021.***

***Live: Thursday Nov 19, 2020 at 11am EST| 8am PST| 4pm GMT| 5pm CET*** Managing polymer variability is critical in developing robust formulations and processes. Cellulose is not only one of the most abundant compounds on Earth, but also one of the most versatile ingredients in the pharmaceutical industry. Learn how its critical material attributes can be customized—from manipulating physical properties like particle size for improved processibility to modifying chemical properties such as substitution and molecular weight, which impacts drug release. This webinar will demonstrate how cellulosic structural property performance fundamentals can help a formulator design the highest quality and most robust drug product formulation. Further, the addition of digital tools can ensure better batch-to-batch consistency and predict other quality parameters, further optimizing a formulation to your needs. *** On demand available after final airing until Nov. 19, 2021.***

***Live: Monday, November 16, 2020 at 1pm EST| 12pm CST| 10am PST*** Register for “Manufacturing Technology: Capabilities for Changing Environments.” Learn how pharmaceutical companies have adjusted in response to the COVID-19 pandemic and continued to grow their business. Join us to explore new technology tools that bridge manufacturing and quality while providing data driven insights for better business decisions. *** On demand available after final airing until Nov. 16, 2021.***

**Thursday, October 29, 2020 at 11am EDT| 8am PDT| 3pm GMT| 4pm CET***An increasing number of new chemical entities (NCEs) present with bioavailability issues. Low bioavailability is associated with increased pharmacokinetic variability in both preclinical species and humans, which can lead to additional development challenges. An expert will discuss API-sparing development techniques and innovative scalable drug delivery technologies that are proven to improve solubility and enhance bioavailability using a minimal amount of API. ***On demand available after final airing until Oct. 29, 2021***

***Live: Wednesday, October 28, 2020 at 11am EDT| 8am PDT| 3pm GMT| 4pm CET*** With over 300 million people worldwide living with one or more identified rare diseases, the development of new treatments to address these unmet clinical needs is an area of significant focus in the pharmaceutical industry. But does the focus on speed mean sacrifices have to be made elsewhere in the development plan for orphan drugs? ***On demand available after final airing until Oct. 28, 2021***

***Live: Tuesday, November 24, 2020 at 9am EST| 2pm GMT| 3pm CET*** Coloring as an aesthetic value for a product is becoming more important for pharmaceutical and nutritional products and helps differentiate between various grades of active ingredients. This webcast introduces the world of easy coloring, answers questions about pigments, pigment blends, and how to color solid- or liquid-dosage forms in an efficient way. Register for this webcast to learn how ready-to-use coloring systems can simplify production process.*** On demand available after final airing until Nov. 24, 2021.***

***Live: November 12, 2020, 11am EST| 8am PST| 4pm GMT| 5pm CET***Formulation strategies for orally administered small molecules can vary widely for early-phase clinical studies and are not always optimal. Sponsors have a wide range of formulation options as they develop program strategies. This webinar will discuss formulation strategies and the advantages that may depend upon drug properties, dosing requirements, and corporate business strategy.*** On demand available after final airing until Nov. 12, 2021.***

***Live: Tuesday November 10, 2020 at 11am EST| 8am PST| 4pm CET| 5pm CET***Sometimes in bioanalysis, solving the fundamental challenge of developing an assay isn’t enough. The webcast will review strategies for solving scientifically challenging problems and providing assays that are robust and reproducible during routine sample analysis.*** On demand available after final airing until Nov. 10, 2021.***

***Live:Friday, November 13, 2020 at 11am EST| 8am PST| 4pm GMT| 5pm CET *** From contaminants in injectables to the fate of APIs in nasal sprays, Raman reveals the identity and distribution of materials in complex formulations. In this webinar we describe the best approaches to characterizing common pharmaceutical samples; from morphologically targeted analysis of filtered particles to full three-dimensional chemical imaging of whole tablets.*** On demand available after final airing until Nov. 13, 2021.***

***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.***