Expertise You Need, When You Need It

In the fast-paced world of medical device innovation, start-ups and established companies alike face a common challenge: access to consistent, high-level expertise without the overhead of full-time staff. Ingenuity Medical Device Research bridges this gap with a tailored subscription service. We specialize in front-end regulatory and clinical development strategy for early-stage neuromodulation and AI-enabled medical devices.

What We Offer

Our subscription model is designed to adapt to your evolving needs, providing flexible, high-impact support across:

Flexible Subscription Tiers

We recognize that every company’s needs are unique. Whether you’re launching a new device, optimizing clinical trials, or developing intellectual property, we have a solution for you:

• Tier 1: Regulatory & Clinical Advisory (Start-up Level)
  • 4-6 hours/month of advisor support
  • Quarterly regulatory roadmap review
  • Document review and recommendations
  • Investor-facing regulatory slide input
  • Email access
• Tier 2: Development Partner Model
  • ​10-20 hrs/month
  • Study design + FDA strategy
  • Vendor selection guidance
  • Board meeting participation
• Tier 3: Embedded Fractional Head of Clinical/Regulatory.
  • ​1-2 days/wek
  • Full strategic oversight
  • DFDA interaction prep
  • CRO oversight
  • Pre-IDE/IDE strategy

Getting Started is Simple

• 3-Step Process :
  1. Step 1: Choose your plan
  2. Step 2: Schedule a kick-off call
  3. Step 3: Start leveraging expert support

Let's Talk