A Tech-Enabled Clinical Future

June 21, 2021 | 10:00AM | EST

A Tech-Enabled Clinical Future — From decentralized clinical trials to AI-enabled drug discovery, technology is forever changing the clinical landscape. All stakeholders need to be positioned to adapt to a future that requires agility, collaboration, and transformation.
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Spotlight

In doping control and forensic toxicology applications, there is a high requirement for sensitivity and quantitative capability as well as an increasing demand for screening approaches, opening the possibility for retrospective analysis. GC triple quadrupole systems are highly valued for their sensi


OTHER LIVE WEBINAR

Essential up-front planning for your clinical trial

June 21, 2021 | 10:00AM | EST

Early, upfront planning of your clinical supply chain is critical to ensuring programs effectively balance risk and cost. When resources are limited and time is essential, early planning can optimize key parameters for study supplies including risk mitigation strategies to avoid stock outs and study delays, minimizing waste with optimized inventory, and forecasting demand to facilitate robust supply planning. Join Simon Caviezel, Program Director for Thermo Fisher Scientific to uncover the benefits and best practices to progress your clinical program smoothly from start to finish.
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The Future of pMDIs: Plasma Technology

June 21, 2021 | 10:00AM | EST

With the introduction of new propellants and more complex formulations, the pMDI canister plays an increasingly significant role in the safe and efficacious delivery of drug to the patient. The relationship between propellant, drug and canister has significantly changed, with the canister no longer being just a safe containment system, but an integral part of the drug delivery itself. During the webinar, participants will gain an understanding of the manufacturing process for H&T Presspart’s pMDI plasma cans and the sustainability benefits of this manufacturing process over other coated can processes such as anodised and FEP coated cans. Participants will also see how H&T Presspart’s inspection and quality process ensures the whole of the internal surface of the can treated with plasma. They will also hear how Plasma can improve inhaler performance and combat drug degradation and drug adhesion, a common problem with many pMDIs. We will show attendees independent data comparing H&T Presspart’s plasma can performance versus other treatment processes as well as discussing which APIs are most suitable for Plasma.
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Flow Chemistry for Accelerated Drug Substance Delivery

June 21, 2021 | 10:00AM | EST

There is no doubt that drug development is a lengthy, costly and uncertain process, riddled with complexities and hurdles. In recent times, the need for accelerated drug development is greater, with added pressure on CDMOs to deliver the goods in a timely, efficient, and agile manner. In this industry, time is not just money, it can impact the entire program. A program which has been through years and years of careful consideration, strategic discussion and pinpoint planning, working with scientific experts to create and develop what is thought to be a medical necessity in order to improve peoples lives. All that being said, it is evident that keeping drug development on track is key, but what if you could accelerate drug development, cutting costs and time. Would you be interested? This webinar discusses drug substance manufacturing in early development and the very concept of being fast, agile and innovative. Paul will take you through the journey of flow chemistry, discussing in depth the benefits of adopting continuous manufacturing over traditional batch manufacturing. As every molecule and development program is different, there is no single manufacturing solution and continuous flow manufacturing is not a panacea, however there are a number of key drivers for choosing to include flow chemistry, some of which are an increased yield and purity, over a shorter period of time which ultimately results in an overall cost saving.
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Spotlight

In doping control and forensic toxicology applications, there is a high requirement for sensitivity and quantitative capability as well as an increasing demand for screening approaches, opening the possibility for retrospective analysis. GC triple quadrupole systems are highly valued for their sensi

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