A Structured Approach to Achieve Shorter Drug Discovery Cycletimes

Biotechs have limited funding, and their investors must regularly be shown constant tangible project progress in the Drug Discovery phase. Biotechs whose projects lag, have their funding and future at risk. Likewise, large pharma must continually re-prioritize its portfolio of Discovery projects, and those that progress fastest typically have the best chance for survival. One irony of the entire drug discovery process is that despite the introduction of (or maybe because of) new “enabling” technologies across biology, chemistry, and computational sciences the average cycletimes of drug discovery projects from target identification to candidate selection has remained relatively static over the years, rather than becoming shorter. Yet some Discovery projects progress faster than others, and a number of factors for reducing cycletime are well within the control of the project investigators. What are these strategies?
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OTHER ON-DEMAND WEBINARS

Making Oral solid dosage forms with galenIQ™ - the sweet-tasting filler binder

During direct compression tablets are manufactured without pre-granulation. Excipients therefore need to be highly effective, controllable and free-flowing.
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Validating Configurable Interactive Response Technology Solutions for Clinical Studies

Bioclinica

In this webinar, the validation of an interactive response technology (IRT) solution built with configurable parameters will be explored. Traditionally, interactive response technology solutions require validation of each study-specific requirement to ensure proper implementation. With the prevalence of configurable interactive response technology solutions where the validation of each configurable parameter occurs within the product, the need for full validation of each requirement within a clinical study has lessened. This webinar will explore how to take advantage of configurations and how to verify them, thereby reducing the effort and timeline required for validation while still maintaining quality within each study.
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Biomarker Driven Drug Development

labroots

Dramatic responses observed with targeted agents in the ‘right’ genomic context have fueled large scale sequencing efforts to identify ‘effective’ treatments for a given patient. In order to expeditiously evaluate a targeted agent against a potential ‘driver’ genetic aberration, so-called Basket trials are conducted.
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Automation in Biopharma and the Impact on Workflows

In this exclusive Drug Digest video interview, Meg Rivers and Feliza Mirasol, Pharmaceutical Technology editors, discuss the benefits of automating entire workflows in analytics versus automating only specific pieces of equipment or only certain processes with Nick Pattinson, head of product, Automata.
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