Discover the comprehensive tools and insights that make Meta-Data-AI the leading platform for healthcare analytics
Comprehensive Coverage of HTA Bodies: NICE, G-BA, HAS, NCPE, ACE, CADTH, ICER, SMC, TLV, and More
Covering indication subtypes, health technologies, comparator interventions, health economics data (including CEA and BIM models), cost and resource metrics, health utilities, HTA report strengths and weaknesses, as well as detailed efficacy and safety insights.
Discover our suite of intelligent AI tools designed to revolutionize healthcare analytics and regulatory compliance
AI-Enabled HTA Insights Platform
The AI-enabled tool delivers in-depth insights from HTA bodies such as NICE, NCPE, SMC, ACE, CADTH, TLV, PBAC, G-BA, HAS, and more.
Users can generate AI-powered summaries to support HTA planning and development, with access to over 100 variables from HTA submissions.
The platform allows unlimited data downloads, while the free version provides access to 30% of the data. All information is detailed, regularly updated, and designed to support informed decision-making.
AI Chatbot for Pharmaceutical Therapies
This AI-enabled chatbot provides users with up-to-date guidelines on the pricing and reimbursement of pharmaceutical therapies.
It covers key agencies including NICE (UK), G-BA (Germany), FDA/ICER (USA), CADTH (Canada), ACE (Singapore), PBAC (Australia), NCPE (Ireland), SMC (Scotland), TLV (Sweden), and many others.
The chatbot answers user queries based on the latest information, including requirements for systematic reviews, health economic models, and real-world evidence—helping users develop HTA submissions that align with current guidelines.
AI Assistant for Medical Devices
This AI-enabled chatbot delivers up-to-date guidance on the registration, pricing, and reimbursement of medical devices.
It covers key regulatory guidelines from the USA, UK, Germany, Canada, Singapore, Australia, Ireland, Scotland, Sweden, Japan, South Korea, China, and more.
The chatbot provides accurate, real-time answers on device classification, registration pathways, clinical and economic data requirements, applicable fees, and other regulatory essentials—empowering users to create compliant, cost-effective submissions while reducing errors and the risk of resubmissions.
Select the plan that best fits your needs and start exploring our powerful analytics platform with transparent, value-driven pricing
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