Webcasts

Thursday, September 28, 2022 at 11am ET | 10am CT | 8am PT Learn the key benefits of continuous OSD production as well as the importance of authenticating OSD products at the dose-level with experts from Syntegon and Colorcon in this episode of the PharmTech Drug Digest Video Series.

Tue, Sep 27, 2022 11:00 AM EDT In this webinar, failure modes that can occur on a perfectly sealed container will be discussed along with how to determine if a CCIT failure is a true container leak or something else

Thursday, September 15, 2022 at 4pm ET | 3pm CT | 1pm PT Partnering with an experienced CDMO can support drug developers’ manufacturing needs and allow them to focus on the core of their developments.

Thursday, September 8, 2022 at 11am EDT; 4pm GMT; 5pm CEST This webinar will highlight the new solubility enhancing Dispersome® technology, which is based on the amorphous stabilization of a given drug using the protein beta-lactoglobulin (BLG) as novel pharmaceutical excipient. Several relevant case studies are presented to showcase the potential of this new technology. Subsequently, the webinar provides a roadmap on how these formulations can be manufactured on a commercial scale. The webinar will also cover the manufacturing of the formulations.

Thu, Aug 25, 2022 11:00 AM EDT Pharmaceutical Technology editors interview aseptic and sterilization experts from Watson-Marlow Fluid Technology Solutions and Cherwell—diving into sterilization, aseptic processing, and the revised EU GMP Annex 1 guidance.

Thursday, ​​​​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.

Thursday, July 14th, 2022 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Join us to learn approaches for the accurate determination of mutagenic azido, NDSRI, and nitrosamine impurities in drug substances and products using LC–MS/MS.

Tuesday, July 12th, 2022 at 11am EDT|8am PDT|4pm BST|5pm CEST Dr. Meike Römer from Grünenthal Pharma, Germany, presents the company’s approach for the evaluation and implementation of transmission Raman spectroscopy for pharmaceutical content uniformity testing.

Thursday June 30, 2022 at 11am ET | 10am CT | 8am PT Cell and gene therapy (CGT) and antibody-drug conjugate (ADC) developers and manufacturers discuss factors that could influence organizations to pursue specific biomolecules for development. Pharmaceutical Technology editors interview experts in CGTs and ADCs in this episode of the Drug Digest video series.

Thursday, June 23, 2022 at 10am ET | 3pm BST | 4pm CEST Join us on June 23 to learn about QC Analysis of Oligonucleotide Therapeutics. One Platform Method for Determining Identity, Purity, and Quantity.

Tuesday, June 14th, 2022 at 7:30am PDT | 9:30am CDT | 10:30am EDT Join Lonza and Quench Medical in a joint discussion about process engineering for the respiratory delivery of gemcitabine to treat lung cancer

Wednesday, 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.

Wednesday, 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.

Thursday April 28, 2022 at 11am ET | 10am CT | 8am PT In this new video series, Drug Digest, the Pharmaceutical Technology editors examine the topic of emerging therapies in more detail, covering subjects such as the challenges of scale, the potential benefits of drug delivery innovation, importance of early analytical studies, the evolution of the regulatory landscape, and differences between regional regulatory requirements. Join the editors as they speak with experts from Regulatory Compliance Associates (RCA), the European Confederation of Pharmaceutical Entrepreneurs (EUCOPE), and others.

April 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!

Thursday, April 21, 2022 at 11am ET | 4pm GMT | 5pm CET This webinar will discuss risk mitigation strategies used to address common challenges during spray dried powder development and give insight into the impact of spray drying on powder properties in terms of manufacturability and downstream processability.

Tuesday, 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.

Thursday, April 14, 2022 at 11 AM EDT | 8 AM PST | 3 PM GMT Suspension formulations – simple or complex? As with many things the answer is “it depends”. This presentation will address the development of suspensions from simple, initial animal study products through complex commercial products.

Thursday, March, 24, 2022 at 4:00pm GMT | 12:00pm EST | 5:00pm CEST From lyophilization to particle engineering. Learn how spray drying can improve solid-form isolation of biopharmaceuticals and expedite your development pipeline, throughput, and therapeutic delivery.

Wednesday, 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.

Wednesday, March 16, 2022 at 11 am EST | 10am CST | 8am PST What will audits and inspections look like once COVID 19 has passed? Attend this webinar to learn how the FDA is approaching inspectional activities depending on the industry.

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.

Tuesday, March 1st 2022, at 11 am EST Making oral solid dosage forms conveniently, using galenIQ™ - the sweet-tasting filler binder.

Monday, 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.

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.***

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.

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.

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.

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.

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.