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BioMeta AI is an advanced AI-powered platform designed to revolutionize how clinical trial study protocols are interpreted and converted into actionable EDC (Electronic Data Capture) database specifications. Acting like a seasoned clinical data manager, BioMeta AI deeply understands complex, unstructured protocol documents — and transforms them into clean, CDASH-compliant deliverables in minutes.
BioMeta AI is designed to work seamlessly with your existing ecosystem:
By automating specification creation, BioMeta AI significantly cuts down manual mistakes and reduces inconsistencies.
The platform supports integration with industry-leading systems such as Medidata, Oracle, Veeva, and more.
With faster database specification development, sponsors can get to the build phase far quicker, reducing overall study timelines.
BioMeta AI offers API support, enabling real-time synchronization with your tools.
No need for manual coding — BioMeta AI delivers a no-code automated workflow, making it accessible even to non-technical users.
Built for future growth — whether you’re running a few studies or a full-fledged clinical program.




Rapidly generate detailed EDC specifications to speed up setup.
Automatically detect changes and regenerate specs with accuracy.
Create clean, compliant documentation for regulatory review.
Accelerate innovation with world-class tech and management teams.
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