We propose establishment of a system for benchmarking of AI tools on private assets (models and data) used for a multiplicity of use cases along the drug discovery, manufacturing, and clinical research value chain. The proposed vendor-neutral system should include benchmark data sets, specifically designed for the named use cases, evaluation metrics, and infrastructure for secure compute and IP protection, that would allow for benchmarking of AI tools without disclosure of the model code and the test data sets.
If team A develops an AI agent application agent-A, and team B develops an AI agent application agent-B, what is the minimal set of information that agent-A and agent-B should exchange such that these two AI agents can work together on the same project? To address this question, we need a standard AI agent-agent communication protocol.
The goal of the project is to develop a metadata standard to describe RWD sources, that can be machine-actionable and enable semantic-based findability and integration.
Such metadata scheme will provide a best and shared way to describe the content, quality, focus and characteristics of a RWD dataset in a way that would enable the understanding of which source is best to answer specific scientific questions.
Following the ‘Carbon Footprint of Decentralized Clinical Trials’ project run by Pistoia Alliance members in collaboration with Sustainable Healthcare Coalition members in the industry Low Carbon Clinical Trials (iLCCT) consortium, the first version of the Clinical Trial Carbon Calculator “Eco Design” tool is to be finalized by the end of 2024 and will be accessible to pharma companies and suppliers.
In the field of biomedical in vivo research, data sharing and repurposing are not commonly practised. One critical element for enabling data sharing and repurposing is the provision of metadata that well describes the raw or primary data.
The current ontologies available to support annotation of experiments and assays (BAO,AFO) don't suffice yet to enable experiment data interoperability and their reusability.
Organisations are increasingly working to standardised ontologies and terminologies to increase the interoperability of data as part of their FAIR data strategy.
Artificial Intelligence (AI) models have been shown to have impressive capabilities in the medical image analysis domain with potential to assist clinicians in their everyday tasks, from the diagnosis to disease monitorisation and surgical planning procedure, thereby enhancing patient care.
Consistent within the direction and intent of the 21st Century Cures Act, the FDA has published guidance for the use of real-world evidence (RWE) in regulatory decision making.
The problem to be solved is the lack of an ontology and/or standard vocabularies in instruments and equipment inventories, which makes the categorizing and querying of these systems difficult.