Webcasts

Capsule formulations to improve delivery of poorly absorbable drugs

Wednesday March 2, 2022 at 11am EST | 4pm GMT | 5pm CET Compounds that are poorly soluble in water are still prevalent in the pharmaceutical industry drug development pipeline. Enabling technologies such as lipid-based formulations (LBF) and amorphous solid dispersions (ASDs) can address these bioavailability limitations, enabling the creation of effective drug products.

Intranasal Drug Delivery: Identifying Challenges & New Product Opportunities

Thursday, February 24, 2022 at 11am EST| 8am PST| 4pm GMT|5pm CET This webinar will discuss the challenges, opportunities, and advantages of intranasal drug delivery and why it has drawn increasing interest as a route of administration. *** On demand available after final airing until November 18, 2022.***

Improving Solubility and Accelerating Drug Development through Integrated Programs

Wednesday, February 23rd 2022 at 11am EST | 5pm CET | Molecules with solubility challenges continue to dominate drug development pipelines, increasing the demand for formulation technologies that can solve these issues. Join CMC Consultant, Peter Timmins, Lonza’s Sr. Research Fellow, David Lyon, and Quotient Sciences’ CSO, Peter Scholes, as they outline how a variety of data-driven strategies and integrated program designs can simplify development processes and reduce costs. Using expert insight and case studies they will showcase how spray drying can solve solubility challenges, and demonstrate how integrating GMP manufacturing and clinical testing can rapidly accelerate development timelines.

Evolving your Micro QC Lab with LIMS integration for Colony Counting

Wednesday, 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.

Quality by Design and Container Closure Integrity

Wednesday, February 8th at 11am EST | 10am CST | 8am PST Industry shifts in container closure integrity (CCI) are driving the next generation of quality control solutions. Understanding the physics behind the technologies and their relation to your application will carve a path of successful CCI assurance.

Dosage Form Design & Patient Compliance: Exploring ODTs as a Patient-centric Solution

Thursday, January 27th 2022 at 11AM EST | 4PM GMT | 8AM PST In this webinar, experts provide an overview of the needs of different patient populations, and examine the common challenges leading to non-compliance. The experts also discuss how an orally dissolving tablet (ODT) provides a solution to address patient challenges and enables potentially more successful treatments.

Drug Digest Video: Pairing the Right APIs and Excipients for Optimizing Formulations

Thursday January 27, 2022 at 11am EST | 10am CST | 8am PST In this new video series, Drug Digest, the Pharmaceutical Technology editors dive into APIs, excipients, and formulation advances, with a focus on pairing the right APIs and excipients for optimizing formulations and efficacy. Join the editors as they speak with experts from Bristol-Myers Squibb, BASF, Thermo Fisher Scientific, Wavelength Pharmaceuticals, and more to determine the most significant factors impacting API and excipient selection as well as the best modalities/drug product forms.

Nanoparticles for Drug Delivery

On 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.