Investment Readiness Agents
CarefulAI provides a suite of specialised AI agents that improve the investment readiness of digital health firms. Each suite of agents addresses particular investment risks. They are maintained by subject matter experts who recognise their agent offers a better way of answering frequently asked questions. The ones shown in blue are free to use.
Ideation Agents
In healthcare it is common that clinical innovators solve their own problems with technology but need to remember to pre-qualify their digital health ideas out further. PreQual helps innovators address this problem and develop a meaningful proof of concept. Newi helps them to develop a new product development plan. Pip helps them to understand the human resource implication of their plan. If their plan involves AI, they are likely to need to manage the risks arising in their supply chain, and PRIDAR was created for this purpose.
Market Access Agents
Clinical innovators often need help understanding the nature of the market they intend to serve beyond the proof of concept stage. Nova helps innovators understand the NHS, and Strat helps them to develop a route to market for their proof of concept. If you are looking to understand the relative competitive advantage of an innovation prior to investment Dill is your tool.
Regulatory Compliance Agents
If the innovation enables systems to diagnose, monitor or manage clinical interventions, it is likely to be classified as software as a medical device. Investments in innovations that do not address software as a medical device regulations result in costly penalties and delays in obtaining CE marks. Sam D supports clinical innovators in their journey to compliance as a medical device, and AutoDeclare agent supports firms in maintaining compliance across multiple jurisdictions, at a fraction of previous costs. Stan enables product support teams to report on clinical standards. If the product involves AI, Reg allows users to of AI to understand their responsibilities. Tracy guides users about the traceability requirements around being a medical device. It Will enable users to explore the effect of innovation on staff's well-being. Emo can be used to mitigate adverse effects associated with a product's use.
User Engagement and Adoption Agents
Engaging users in the design, development and monitoring of digital healthcare products is good design practice. This is often a compliance requirement for regulations. To increase adoption rates clinical innovators need to understand the motivations around a user experience. Mo enables motivational interviewing to be undertaken at scale. If changes in user behaviour need to be understood Bev can provide actionable insights.
Privacy and Security Agents
Di enables clinical innovators to create a data protection impact assessment, which law in the UK and EU requires. Miti supports technical risk mitigation. CSO guides clinical innovators in the responsibilities and activities of Clinical Safety Officers around using risk and mitigation registers.
Clinical Trials Agents
Clarion enables clinical innovators to design and execute efficient and compliant clinical trials, essential for demonstrating new health technologies' efficacy and safety. Compli enables innovators to understand if their clinical trials are comparable to those with regulatory compliance.
Ideation Agents
In healthcare it is common that clinical innovators solve their own problems with technology but need to remember to pre-qualify their digital health ideas out further. PreQual helps innovators address this problem and develop a meaningful proof of concept. Newi helps them to develop a new product development plan. Pip helps them to understand the human resource implication of their plan. If their plan involves AI, they are likely to need to manage the risks arising in their supply chain, and PRIDAR was created for this purpose.
Market Access Agents
Clinical innovators often need help understanding the nature of the market they intend to serve beyond the proof of concept stage. Nova helps innovators understand the NHS, and Strat helps them to develop a route to market for their proof of concept. If you are looking to understand the relative competitive advantage of an innovation prior to investment Dill is your tool.
Regulatory Compliance Agents
If the innovation enables systems to diagnose, monitor or manage clinical interventions, it is likely to be classified as software as a medical device. Investments in innovations that do not address software as a medical device regulations result in costly penalties and delays in obtaining CE marks. Sam D supports clinical innovators in their journey to compliance as a medical device, and AutoDeclare agent supports firms in maintaining compliance across multiple jurisdictions, at a fraction of previous costs. Stan enables product support teams to report on clinical standards. If the product involves AI, Reg allows users to of AI to understand their responsibilities. Tracy guides users about the traceability requirements around being a medical device. It Will enable users to explore the effect of innovation on staff's well-being. Emo can be used to mitigate adverse effects associated with a product's use.
User Engagement and Adoption Agents
Engaging users in the design, development and monitoring of digital healthcare products is good design practice. This is often a compliance requirement for regulations. To increase adoption rates clinical innovators need to understand the motivations around a user experience. Mo enables motivational interviewing to be undertaken at scale. If changes in user behaviour need to be understood Bev can provide actionable insights.
Privacy and Security Agents
Di enables clinical innovators to create a data protection impact assessment, which law in the UK and EU requires. Miti supports technical risk mitigation. CSO guides clinical innovators in the responsibilities and activities of Clinical Safety Officers around using risk and mitigation registers.
Clinical Trials Agents
Clarion enables clinical innovators to design and execute efficient and compliant clinical trials, essential for demonstrating new health technologies' efficacy and safety. Compli enables innovators to understand if their clinical trials are comparable to those with regulatory compliance.
Feedback
You can provide feedback on individual agents by following the link beneath the agent you have used. If you would like to see other agents provided, or if you wish to have your own. Let us know
Investment Management
When it comes to managing investments, nothing beats people with experience. To this end, CarefulAI has partnered with.
Experto Crede, for route to market support for global digital solutions
XR Health for UK deployment of digital health solutions
Blum Health Tech for UK software development
Experto Crede, for route to market support for global digital solutions
XR Health for UK deployment of digital health solutions
Blum Health Tech for UK software development
