Hill Research helps companies of all sizes bring products to market faster, and more efficiently and maintain compliance. Our solutions provide data, software, services, and an extensive ecosystem to support your most critical functions from R&D through commercial.
From trial design to FDA submissions, we provide end-to-end AI-driven solutions, including intelligent decision support, compliance optimization, and safety predictions. Powered by a multi-agent large language model (LLM) tree, we enable pharmaceutical companies to shorten clinical trial cycles, streamline trial operations, and significantly increase drug approval success rates.
“The Hill Research team excels at transforming GenAI expertise into impactful solutions, revolutionizing healthcare across drug discovery, patient recruitment, and evidence generation with a holistic approach. I’m excited to continue our collaboration.”
“Hill Research leverages AI to boost efficiency and success rates in pharma, with a human-centered approach that enhances decision-making and team confidence. We’re excited to continue collaborating.”
TheraGPT is an extensible agentic AI platform built to solve complex clinical data and documentation challenges. Thanks to its modular structure, it can be offered as an all-in-one solution to pharmaceutical clients.
Automating CRF annotation, patient recruitment, compliance, and data analysis, making those tasks up to 20x faster
Achieving 98%+ precision through fine-tuned AI models and continuous learning
Whether it’s proprietary company data or protected health information, modules are built to avoid unwanted data releases
Automatic desensitization of medical information to ensure compliance with regulations using advanced Natural Language Processing techniques.
Our Data Compliance Agent automatically scans documents, detects sensitive data, obscures it, and returns anonymized data that follows the regulations supplied (e.g. HIPAA). It also securely stores relationships, allowing de-anonymization if needed.
Extracting clinical information from various sources to support regulatory filings and scientific decisions.
There are massive amounts of information available to inform clinical trials or identify new targets, and it is difficult to query it at scale. Using our Natural Language Processing solutions, we can transform large amounts of text data into searchable databases, and extract information relevant to your needs.
Automates the patient recruitment process for clinical trials
This clinical trial patient recruitment agent can automatically organize, summarize, and learn the treatment information of past patients, and apply the learned treatment experience to the treatment of new patients; it can also provide real-time information for clinical trials. Effective clinical trial patient recruitment information, thereby improving the efficiency of screening characteristic patients; providing Real World Evidence (RWE) for off-label use of traditional drug sheets; at the same time, it can also guide local medical insurance bureaus to regulate overtreatment issues and more.
Automating the preparation of documents for FDA submissions.
During a trial, Case Reporting Forms (CRF) need to be annotated in compliance to CDISC standards before submitting to the FDA. This AI Agent works closely with human experts to automate the tedium of producing consistent and compliant annotated CRFs, significantly increasing efficiency.
Extracting clinical information from various sources to support regulatory filings and scientific decisions.
This include both Internal knowledge base and Public knowledge base, the agent is able to search and analyze over 1M clinical documents within 5 seconds. No prior knowledge necessary use the clinical analytics system.