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Medical Text Processing on Google Cloud

The FDA has a history of using real world evidence (RWE) as an integral component of the drug approval process. Moreover, RWE can mitigate the need for placebos in some clinical trials. The clinical records that make RWE evidence useful, however, often reside in unstructured formats, such as doctor’s notes, and must be “abstracted” into …

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Graph neural networks in TensorFlow

Posted by Dustin Zelle, Software Engineer, Google Research, and Arno Eigenwillig, Software Engineer, CoreML Objects and their relationships are ubiquitous in the world around us, and relationships can be as important to understanding an object as its own attributes viewed in isolation — take for example transportation networks, production networks, knowledge graphs, or social networks. …

Public cloud vs. private cloud vs. hybrid cloud: What’s the difference?

It’s hard to imagine a business world without cloud computing. There would be no e-commerce, remote work capabilities or the IT infrastructure framework needed to support emerging technologies like generative AI and quantum computing.  Determining the best cloud computing architecture for enterprise business is critical for overall success. That’s why it is essential to compare …

TFGNN2520hero

Graph neural networks in TensorFlow

Posted by Dustin Zelle, Software Engineer, Google Research, and Arno Eigenwillig, Software Engineer, CoreML Objects and their relationships are ubiquitous in the world around us, and relationships can be as important to understanding an object as its own attributes viewed in isolation — take for example transportation networks, production networks, knowledge graphs, or social networks. …

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Accenture creates a regulatory document authoring solution using AWS generative AI services

This post is co-written with Ilan Geller, Shuyu Yang and Richa Gupta from Accenture. Bringing innovative new pharmaceuticals drugs to market is a long and stringent process. Companies face complex regulations and extensive approval requirements from governing bodies like the US Food and Drug Administration (FDA). A key part of the submission process is authoring …