Accelerating Life Sciences with Generative AI
Octozi uses large language models to streamline regulatory submission, generate clinical documentation, conduct quality control, and more
A leap forward in life sciences x AI
Generate documents in minutes
Save countless hours manually writing documents needed for IND submission, regulatory briefings, and site operations.
.png)
AI agents do quality control so you don't have to
Continuous quality control minimizes sources of clinical trial delays, mistakes, and costly amendments to protocols.
Confident, quick responses to regulatory authorities
Get fast access to contextual, scientific backed, sourced responses to the regulatory authorities at any stage of your clinical trial
Why Octozi?
01 / TIME
Cut the weeks it takes to create all the documentation needed to get your trial underway.
02 / COSTS
Reduce costs associated with medical writing and document preparation. Get your drug to market faster.
03 / QUALITY
Detect errors across your data and documentation to help eliminate risks to your study timeline and costly amendments that will take your trial off course.
Pioneers in AI for biotech
Scalable, extensible platform
Platform built to handle the needs of biotech startups, large pharma, and CROs across Phase I - IV trials and a broad range of therapeutic areas
Powered by GPT4 & LLMs
Powered by OpenAI's GPT-4 and other large language models (LLMs) providing incredible performance.
Security and Privacy
Your data remains your data and is not shared or distributed to third parties.