Webcasts

An Integrated Approach to Spray Drying: From Scale-Up to Manufacturing

The application of a phase-appropriate quality-by-design (QbD) framework increases the understanding of the interplay between the process parameters of spray drying and product quality that, when applied during scale-up, increases the chances of a successful outcome of the commercial manufacturing process. Live: Tuesday, November 19, 2019 at 10am EST | 9am CST | 3pm GMT | 4pm CET On demand available after airing until Nov. 19, 2020 Register free

Replacing Settle Plates with Active Air Sampling

Join this discussion with experts about implementing active air microbial monitoring in sterile cleanrooms. Learn about changes that can save time and money and reduce the risk of product contamination. Live: Wednesday, Nov.13, 2019 at 10am EST | 9am CST | 3pm GMT | 4pm CET On demand available after airing until Nov. 13, 2020 Register free

How to Approach Preparative LC for Compound Purification in the Research and Development Laboratory

Ready to scale-up your analytical LC method to prep LC and not sure where to start? Join our webcast to discover how to select the right preparative HPLC column to meet your application needs. Live: Thursday, Nov. 7, 2019 at 11am EST | 8am PST | 4pm GMT | 5pm CET On demand available after airing until Nov. 7, 2020 Register free

Choosing The Right CDMO For Late-Phase Clinical Trials

For many pharmaceutical companies that do not have their own facilities, choosing the right partner for late-phase clinical trials and commercial production is a critical aspect in the management of parenteral products. Join Christy Eatmon, Global SME, Sterile Drug Products at Thermo Fisher Scientific, where she will lead a webcast that will offer insight into the importance of looking for a partner with extensive experience in the parenteral arena. Live: Wednesday, Oct. 30, 2019 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after final airing Oct. 30, 2020 Register free

Data Integrity and the Next Level of Connectivity in a Modern Lab

Why is laboratory data integrity a hot topic for bio/pharma companies and regulators? Get insights on challenges and solutions in the paperless laboratory in this webcast. Live: Tuesday, Oct. 29, 2019 at 11am EDT | 8am PDT| 3pm GMT| 4pm CET On demand available after airing until Oct. 29, 2020 Register free

New Research Revealed on a Promising Functional Alternative to Surfactants within Biologic Formulations

New research shows KLEPTOSE® BIOPHARMA as a potential functional alternative to surfactants within biologic formulations, learn more from Roquette’s experts Peter Ferguson and Pen Tao. Live: Tuesday, Oct. 29, 2019 at 9am CDT | 10am EDT | 2pm GMT | 3pm CET On demand available after airing until Oct. 29, 2020 Register free

A Roadmap for Early Development to Commercial Manufacturing

Join this webcast to learn how to avoid common pitfalls in the tech transfer and scale-up process using an integrated approach. Live: Thursday, Oct. 24, 2019 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Oct. 24, 2020 Register free

An Integrated Approach to Rapidly Delivering Bioavailability-Challenged Small Molecules to the Clinic

Oral administration of small molecules has become increasingly difficult due to a majority of new candidates demonstrating poor aqueous solubility. Dr. David Lyon will discuss a proven model-based technology selection methodology for poorly soluble molecules and an integrated formulation approach to minimize first-in-human timelines. Live: Wednesday, Oct. 23, 2019 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Oct. 23, 2020 Register free

New Draft USP Chapter for Water Activity Measurement

The pharmaceutical industry has used Karl Fisher titration to measure total water content in oral solid dosage forms for 30-years. Learn how USP , a new compendium for water activity measurements, recommends water activity methods for providing unique data and insights into formulation development, packaging selection, manufacturing, and long-term stability of pharmaceutical solids. Live: Tuesday, Oct. 22, 2019 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Oct. 22, 2020 Register free

Workflow Breakthroughs that Are Improving Data Quality and Efficiency and Changing Pharmaceutical Analysis

Join us for this webcast to learn about new technologies that can dramatically reduce the risks around routine pharmaceutical analysis while also reducing the time required from hours and days to minutes. Live: Europe: Wednesday, Oct. 16, 2019 at 9am EDT | 2pm BST | 3pm CEST US: Wednesday, Oct. 16, 2019 at 2pm EDT | 1pm CDT| 11am PDT On demand available after final airing until Oct. 16, 2020 Register free