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Technology Forum: The Next Steps for Pharma Manufacturing Efficiency and Effectiveness
September 15th 2021Wednesday, September 15, 2021 at 10am EDTDrug manufacturing demands and increased regulatory oversight are prompting pharmaceutical manufacturers to consider new processes for oral solid dose and aseptically processed drugs. A cross-section of industry experts will offer insight on emerging trends, technologies, and processes in this Technology Forum.
First-in-Human to Commercial: A Microdosing Journey
August 26th 2021Thursday, August 26, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST This webcast will explore the benchmark practices for rapid progression from first-in-human to large-scale commercial manufacture for microdosing API. Micro-dosing at a commercial scale made effortless.
Using Artificial Intelligence in a Digital Twin Strategy
August 23rd 2021Monday, August 23, 2021 at 2pm EDT | 1pm CDT | 11am PDT What do Plato, Roombas, and digital twins for pharma manufacturing have in common? Learn how digital twins, powered by artificial intellingence, can reproduce conditions happening in physical assets to identify and optimize manufacturing process variables, predict outcomes, and empower to bio/pharma companies take action.
Dry Powder Inhalation Delivery of Monoclonal Antibodies
July 22nd 2021Thursday, July 22, 2021 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST Local delivery of monoclonal antibodies to the lung is enabled by spray drying to manufacture stable, respirable dry powders. An inhaled formulation of bevacizumab was effective in vivo, reducing tumor burden in a rat model of non-small cell lung cancer.
Meeting Development and Manufacturing Demands for Emerging Therapies
July 21st 2021Wednesday, July 21, 2021 This Technology Forum will explore the current state of commercialization for cell and gene therapies and the patient and physician perspective, as well as the need for technologies, processes, and strategies to ensure competent delivery of these treatments to patients.
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*
Parenteral Packaging for Cartridges in Drug Delivery Devices
June 22nd 2021*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*
Transforming Water to Meet Strict and Consistent Microbial Control While Reducing OPEX
June 15th 2021*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*
PPD Laboratories’ Suzhou, China Lab Virtual Grand Opening
June 9th 2021*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*
Challenges with Verification of Compendial Chromatographic Methods
May 27th 2021*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*
Bridging the Digital Divide to Advance Bio/Pharma Manufacturing and Quality: A Technology Forum
May 25th 2021*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*
The 2D-LC System of Your Dreams - The Innovative Take on Vaccine Research
May 19th 2021*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*
Enabling Formulations of Poorly Absorbable Drugs with Capsule Solutions
May 18th 2021Two 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*
Using AI for CAPA and Root-Cause Investigations
May 6th 2021*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*
Is My Molecule Suitable for an Orally Disintegrating Tablet?
May 5th 2021*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*
Strategies for Intensified Bioprocessing: From Seed Train to High Cell Density Clarification
April 29th 2021*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.
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.***
Technology Forum Series: Strategies to Prevent Drug Shortages and Resolve Capacity Challenges.
***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.
Drug Manufacturing During a Global Pandemic
March 31st 2021***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.***
The Art of Changing QC Testing Processes to Build Effective Data Integrity Compliance
March 30th 2021***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.***
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.***
