I'm building a regulatory AI tool for medical writers and want honest feedback before I launch it
Hey guys,
I'm building a tool called Vera and before I launch I genuinely want feedback from people who actually work in this field.
The main thing it does is document review. You upload a clinical study or any regulatory document and it comes back flagging compliance issues, structural gaps and ICH guideline mismatches with tracked changes and citations attached. The idea is it handles the tedious baseline pass so you're starting from a better place instead of doing a full manual sweep yourself.
The other thing that pushed me to build this was that most people in this field can't put client documents into ChatGPT. Unpublished studies, proprietary data, it can't go into a public tool. This keeps everything in your own account.
There's also a chatbot built on current CFR and ICH guidelines so if you have a quick regulatory question you can just ask it and get a cited answer without digging through the federal register.
A few things I genuinely want to know:
- Is the manual reformatting and compliance checking actually where a lot of your time goes?
- Does this sound like something you'd actually use or is it solving the wrong problem?
- What would you change or add to make it more useful for your workflow?
Happy to answer any questions about it.