Webcasts

Dominic Warrino and John Perkins of KCAS will provide an overview of recent developments in the pharmaceutical and bioanalytical industries outside of what is being done to address COVID-19. They will also examine case studies looking at the scientific challenges that KCAS continues to see on a daily basis. Live: Friday, May 29, 2020 at 11am EDT | 8am PDT | 4pm BS T| 5pm CEST On demand available after airing until May 29, 2020 Register free

In this exclusive webcast, MasterControl’s Product Management Director Sue Marchant examines why document dependency has become a hindrance to manufacturers and how companies can successfully chart a clear path to digital and data maturity. She also explains the drivers behind the industry’s shift away from document-centered quality management and explores trends relating to digital quality management. Live: Thursday, May 28, 2020 at 2pm EDT| 1pm CDT| 11am PDT On demand available after airing until May 28, 2021 Register free

Looking for the right approach to advance your small molecule drug candidate? Philip Jones from MD Anderson Cancer Center shares thoughts on how to bring drug candidates to Phase I clinical trials. Live: Wednesday, May 27, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 27, 2021 Register free

Learn how biopharmaceutical development and production can be more efficient by using modular technology. Live: Wednesday, May 27, 2020 at 2pm EDT | 1pm CDT | 11am PDT On demand available after airing until May 27, 2021 Register free

The COVID-19 pandemic should prompt bio/pharma facilities to assess how the potential spread of the virus may impact different areas of development and manufacturing facilities, employees, visitors, and product. Learn about strategies for evaluating practices at existing facilities and options for designing new facilities that can accommodate future needs, including flexibility requirements and any emerging threats. Live: Tuesday, May 26, 2020 at 2 pm EDT| 1pm CDT| 11am PDT On demand available after airing until May 26, 2021 Register free

Learn how to reduce the number of steps and resources needed to assure chemical and structural integrity throughout drug development process. See where efficiencies can be gained in analytical methods development and transfer to QC and manufacturing while staying compliant with cGxP. Thursday, May 21, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after final airing May 21, 2021 Register free

For drug-device combination products, the compatibility of the drug and device components requires analysis of many factors. In this webcast, learn about regulations and drug-device compatibility assessment steps that are necessary to protect patients. Live: Tuesday, May 19, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 19, 2021.

This PharmaTalks session focuses on how the integration of Patheon into Thermo Fisher Scientific has resulted in unique opportunities for innovation, collaboration, and technology development, and how we are leveraging the Thermo Fisher ecosystem to develop and improve a platform for biopharmaceutical manufacturing Live: Tuesday, May 19, 2020 at 8am EDT Register free

Learn from the experts on how to best combine supply-chain management and logistics expertise to build a nimble and efficient operation that can help to mitigate risks such as those brought on by the COVID-19 pandemic. Live: Monday, May 18, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing May 18, 2021 Register free

This webcast will describe raw material verification testing through transparent and non-transparent packaging using the new Agilent Vaya handheld Raman system. True through-barrier analysis removes the need for sampling, increasing testing throughput without increasing costs-from clear glass vials to multilayer paper sacks. Live: Europe Broadcast: Thursday, May 14, 2020 at 9am EDT | 2pm BST | 3pm CEST US Broadcast: Thursday, May 14, 2020 at 2pm EDT | 1pm CDT | 11am PDT Asia Pacific Broadcast: Friday, May 15, 2020 at 8:30am IST | 11am CST | 12pm JST | 1pm AEST On demand available after airing until May 14, 2021.

Discover how genotoxic nitrosamine impurity analysis can be performed in a cost-sensitive manner using liquid chromatography with high-resolution mass spectrometry to deliver robust, sensitive, and high-throughput assays under GMP conditions. Wednesday, May 13, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing May 13, 2021 Register free

Gain insight from Nicholas Hall, the Consumer Healthcare Products Association, and Catalent into the performance of the OTC market, some of the innovation trends and opportunities that are emerging, and the impact of OTC monograph reform on future developments. Live: Tuesday, May 5, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 5, 2021 Register free

The global coronavirus pandemic has tested the abilities of bio/pharmaceutical companies to develop new therapies and maintain-or even accelerate-production of existing drugs. In this webcast, experts will discuss business continuity practices, regulatory compliance, and supply chain management under current-or future-emergency conditions. Live: Tuesday, Apr. 28, 2020 at 11 am EDT | 10 am CDT | 8 am PDT On Demand: available after airing until Apr. 28, 2021 Register free

Don’t just rely on packaging to deter the counterfeiting of your drug products. In this webcast you will discover how patient-centric, on-dose authentication can protect products and mitigate counterfeiting and product diversion. Just imagine uniquely encoded micro taggants applied to your product and being able to authenticate right through the supply chain to the patient level…..now that’s smart ! Live: Thursday, Apr. 23, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 23, 2021 Register free

Looking to eliminate trial and error in the early stages of formulation development? Learn how the ZoomLab™ Virtual Formulation Assistant, can predict and optimize an oral solid dosage drug formulation more efficiently than with traditional approaches. Live: Tuesday, Apr. 21, 2020 at 9am EDT | 2pm BST | 3pm CEST On Demand: available after airing until Apr. 21, 2021 Register free

Looking for a fast pathway to an investigational new drug application (IND) for your new drug candidates? This webcast will discuss strategies to select the most developable molecules and quickly develop an IND-ready formulation within 8–12 weeks using real-world case studies. Live: Wednesday, April 15, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 15, 2021 Register free

Join us on April 7th, for part one out of our three-part series, which will focus on innovations in the manufacturing of parenteral packaging components to address the demanding needs for packaging sensitive drugs, such as biologics. Live: Part I: Tuesday, Apr. 7, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after airing until Apr. 7, 2021 Register free

This webcast will cover physicochemical requirements and biological oral delivery barriers for peptides. Learn innovative approaches to derisk pharmaceutical development and increase the success rate of the first in human trials. Live: Wednesday, Apr. 1, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 1, 2021 Register free

Join Ian Olmsted, PhD, to learn how you can perform ignition and drying methods more safely, without sacrificing data quality or workflow. He will explore the hazards associated with sulfated ashing and moisture content analysis in the pharmaceutical industry. Live: Thursday, Mar. 26, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after airing until Mar. 26, 2021 Register free

Learn what the common equipment bottlenecks are and how engineering developments can maximize equipment availability. Experts will provide insight into how to minimize cycle, set-up, and changeover times and how to define optimal parameters for each process step. Live: Tuesday, Mar. 24, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after airing until Mar. 24, 2021 Register free

Learn techniques on getting your drug product to market faster and more efficiently. Live: Thursday, Mar. 19, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after airing until Mar. 19, 2021 Register free

Imagine a blue dye test that uses a tracer gas in place of the dye. Headspace gas ingress testing is a robust detection method of critical leaks. Drug developers considering an upgrade to blue dye testing can learn more about this test method in this webcast. Live: Wednesday, Mar. 18, 2020 at 11:30am EDT | 8:30am PDT | 3:30pm GMT | 4:30pm CET On Demand: available after airing until Mar. 18, 2021. Register free: http://www.pharmtech.com/pt_w/closure

Complex liquids can be problematic for scale-up and manufacture. Learn how the experts at Catalent have found solutions for the most challenging liquid formulations. Live: Tuesday, Mar. 17, 2020 at 1pm EDT | 12pm CDT | 10am PDT On demand available after airing until Mar. 17, 2021 Register free

Join us for an informative webcast on March 12th at 11am EDT as we discuss the full capabilities of the Lonza Capsugel® Products and Services Portfolio. Our offerings include high-quality capsules, both in gelatin and specialty polymers, a premier portfolio of equipment, unparalleled industry and regulatory knowledge, and more. Live: Thursday, Mar. 12, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after airing until Mar. 12, 2021 Register free

During this webcast, we will explore the use of a portable XRF instrument that moves the point of testing salt samples to the warehouse and allows sample results to be available in less than a minute. Live: Wednesday, Mar. 11, 2020 at 10am EDT | 9am CDT | 2pm GMT | 3pm CET On demand available after final airing Mar. 11, 2021 Register free

How can you overcome clinical import and export challenges within the Asia-Pacific region? Join Catalent’s Julie Delaney and Rognvald Lamb as they present the advantages of using Singapore as an APAC clinical supply hub. Live: US & Europe Broadcast: Wednesday, Feb. 19, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET Asia-Pacific Broadcast: Thursday, Feb. 20, 2020 at 8:30am IST | 11am CST | 12pm JST On demand available after airing until Feb. 19, 2021 Register free

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

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