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Webinar
Join us for an enlightening webinar where we delve into the profound influence leaders have on the mental well-being and performance of their team members through their management approaches.
In this dynamic session, we will explore the transformative power of in vitro assays and in silico predictive analysis, replacing traditional animal models with ethical, efficient, and scientifically advanced alternatives
This event will provide insight on how copyrighted materials are retained and reused in AI systems, including large language models
This presentation will introduce some of the approaches SciBite is taking to enhance and leverage knowledge graphs in the context of AI
This project aims to build a pharmaceutical (CMC) process ontology based on the ISA88/95 framework to standardize laboratory and plant production process recipes to establish standardized definitions, facilitate digital technology transfers, and integration with execution systems.
We know enough about the LLM technology at this time to move it from popular hype into production. We are, however, still at the beginning of this journey. What does biopharma research need to focus on to ensure they are implementing LLMs effectively?
ACMD has made recommendations to reduce barriers to research, using compounds described by the third generation synthetic cannabinoid receptor agonists generic definition. This webinar will cover the background and how the Pistoia Alliance Controlled Substance Compliance and Shipping (CSCS) expert community investigates the potential implications of such proposals.
In this webinar, we look at how data quality affects the performance of LLMs. For this, we assess how LLM-powered AI agents query across three versions of the same gene expression corpus, but with varying degrees of quality
Join us for this inaugural update on the newly formed Strategic Priorities of the Pistoia Alliance, followed by a 30 minutes Q&A with our panelists
Join us to learn more about our IDMP-O initiative. Our newly launched IDMP-O version 1.0 covers all five ISO IDMP standards, enabling a broad range of use cases around substance identification, regulatory processes integration with manufacturing, supply-chain analytics, therapeutic indications, representation of jurisdiction-agnostic medicinal products and pharmacovigilance.
Why is managing change so critical in digital transformation? What are some of the challenges in a successful rollout? How do you manage change effectively when digital transformation is just one of the changes that people are experiencing? What are the key success factors in effective digital transformation?
