Webcasts: Pharmaceutical Analysis
>Webcasts: Pharmaceutical Analysis
Allowing You to do More with Less: The TRS100 Transmission Raman System
July 21st 2022Thursday, July 21st, 2022 at 11am EDT|8am PDT|4pm BST|5pm CEST 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.
Extractables and Leachables: Trends and Future Directions Part II A roundtable discussion
May 25th 2022Wednesday, May 25, 2022 at 11am EDT|8am PDT|5pm CEST|4pm BST In the last few years, the issuance of the ISO 10993-18:2020 medical device guidance and several high-profile publications and round robin studies have resulted in the FDA increasing scrutiny of E&L analyses for both drugs and devices. Join our panel of industry experts to discuss these changes and to learn the direction E&L studies may take in the future.
The Ever-Changing World of Extractables and Leachables, Part 4, A Free Virtual Conference
May 18th 2022Wednesday, May 18th, 2022 at 3pm BST | 10am EDT | 4pm CEST | 7am PDT Join global industry and regulatory experts as they discuss current E&L hot topics on pharmaceuticals, biopharmaceuticals and medical devices.
Gaining Critical Insights, Automation, and End-to-End Connectivity From Your Lab Data
April 27th 2022April 27th, 2022 at 11am EDT | 8am PDT | 3pm GMT | 10am CDT Transform Data into Scientific Discoveries. PerkinElmer’s World Class eNotebook and Scitara DLX Live Demo! Signaling the Future with True Informatics Data Mobility. Watch our live demonstration on how to achieve true data mobility!
Cut Pharma Maintenance Costs and Improve Asset Efficiency with AI and Advanced Analytics
April 19th 2022Tuesday, April, 19, 2022 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Be assured they have the most uptime possible to keep production on track! Register for this webinar to learn how advanced technologies can help ensure complete asset integrity, guarantee optimal facility conditions (such as temperature, humidity, and vibrations), predict the expected lifespan of equipment and track the energy an asset has consumed and its CO2 emissions.
An Expert Panel Discussion on Best Practices When Transitioning from CSV to CSA
March 23rd 2022Wednesday, March 23, 2022 at 11am EST | 10am CST | 8am PST The goal of this webinar is to provide clarity on what the upcoming computer software assurance (CSA) guidance means for life sciences companies and what they can do to start preparing. Leading experts from Biogen, Vertex, Alkermes and Verista will share their advice and best practices to ensure a successful rollout.
Laying the Foundation for Smart Manufacturing While Solving Today’s Tough Challenges On Demand
February 28th 2022Monday, February, 28, 2022 at 9am EST | 8am CST | 6am PST Realizing benefits from Smart Manufacturing technologies doesn’t have to be long-term prospect. Solve today’s manufacturing challenges while laying the foundation for tomorrow’s plant.
Evolving your Micro QC Lab with LIMS integration for Colony Counting
February 16th 2022Wednesday, February 16, 2022 at 9 AM EST | 6 AM PST | 2PM GMT | 3 PM CET & 11AM EST | 8AM PST | 4PM GMT | 5PM CET How are you approaching Pharma 4.0 and the QC Lab of the future with automation? Join us for an informative Webinar on the benefits of end-to-end integration with LIMS and QC Micro automation.
Nanoparticles for Drug Delivery
January 26th 2022On Demand Webcast Nanoparticles have unique properties that are manipulated to create novel solutions, such as innovative drug delivery systems seen in today’s Covid-19 mRNA vaccines. This webinar explores the analytical techniques used for nanoparticle characterization and its growing significance in drug delivery systems.
Introduction to High Resolution Integrated Weighing
January 18th 2022Tuesday, 1/18/22 at 11am EST | 8am PST | 5pm CET | 4pm GMT In this presentation we look at the products available to support projects where high resolution weight determination is essential. We will also explain what is important when designing a system that requires an integrated weighing solution and the various factors that can influence the performance and final results.
Why Biotech and Pharma Need GxP for their Digital Transformation Projects Now
December 20th 2021Monday December 20, 2021 at 11am EST | 10am CST | 8am PST Pharmaceutical manufacturers are under increasing pressure to fast-track technological innovation while remaining compliant. What are the correct steps to reaching operational intelligence with end-to-end data integrity?
Analytical-Scale Prep, Semi-Prep, Process Scale Preparative Chromatography: To Infinity and Beyond!
October 26th 2021Tuesday, October 26, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Are you planning to turn your analytical HPLC method into a purification method? Are you converting your analytical-scale purification method to semi-prep or production scale? Learn how to set appropriate purification goals for purity, yield and throughput and what type of equipment will best fit your application.
Extractables and Leachables: Trends and Future Directions A roundtable discussion
September 28th 2021Tuesday, September 28, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST In the last few years, the issuance of the ISO 10993-18:2020 medical device guidance and several high-profile publications and round-robin studies have resulted in the FDA increasing scrutiny of E&L analyses for both drugs and devices. Join our panel of industry experts to discuss these changes and to learn the direction E&L may take into the future.
Accelerate Time to Market via Virtual Formulation Design: A Step-By-Step Approach
June 23rd 2021*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*
Strategies to Simplify the Evaluation of Pharmaceutical Excipients
April 28th 2021***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.***
Unpacking USP <922> & Water Activity’s Role in the Pharmaceutical Industry
March 30th 2021***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.***
The Importance of Titrations in Pharmaceutical Analysis: From the Basics to the Modern Method
February 24th 2021***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.***
