video1.0<iframe src="https://www.loom.com/embed/1868fe9f1812435bbc3247f6501a9bd9" frameborder="0" width="1216" height="912" webkitallowfullscreen mozallowfullscreen allowfullscreen></iframe>9121216Loomhttps://www.loom.com9121216https://cdn.loom.com/sessions/thumbnails/1868fe9f1812435bbc3247f6501a9bd9-f0a39e775e27fe33.gif245.035In this video, I walk you through our innovative system that streamlines the pre-clinical safety review process required by the FDA before drug trials. We can significantly reduce the time and cost associated with manual reviews, which typically range from $15,000 to $25,000 and take three to four weeks. Our AI-driven platform extracts critical data, assesses compliance against 95 rules derived from ICH and FDA guidelines, and generates comprehensive reports. I also highlight the importance of addressing any flagged issues to avoid clinical holds, and I encourage you to upload any additional documents needed for a complete assessment. Let's ensure we meet all requirements efficiently and effectively.