🛡️ Is Your AI Health Tool Market-Ready? This New Free Toolkit Tells You Instantly
📍 Are you developing AI in healthcare? Hoping to scale into the NHS or EU markets? Read this before you go any further.
At healthtechnologyconsulting.com, we’ve just launched a powerful Healthcare AI Regulatory Readiness Audit Template – and it’s completely free to download.
This workbook condenses everything you need to self-assess your compliance with:
✅ MHRA Medical Device rules
✅ NICE Evidence Standards Framework (ESF)
✅ EU AI Act 2024 (yep, the high-risk AI one)
✅ GDPR / UK Data Protection
✅ NHS AI Knowledge Repository standards
🚀 What You’ll Get
A structured checklist to evaluate your AI product's regulatory fitness
Clause-by-clause coverage of every compliance domain (from DPIAs to CE marking)
An interactive action-plan builder to identify gaps and mitigate risks
Embedded links to NHS, ICO, NICE and MHRA source docs – no fluff, all signal
⚠️ Why It Matters
The UK and EU are tightening oversight of digital health and AI tools. NHS buyers, clinical leads, and procurement boards increasingly expect bulletproof compliance before pilot even begins.
If your product doesn’t tick the boxes now, you risk being locked out of the market later.
🧠 Built by Experts, For Builders
This isn’t a generic legalese guide. It’s a hands-on toolkit that reflects what senior compliance leads build manually over weeks – now available as a plug-and-play workbook.
💼 Ideal for:
Start-ups preparing for NHS DTAC or EU CE approval
Scale-ups chasing Series A with regulatory traction
Digital health teams wanting clarity before clinical deployment
