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, offering unparalleled expertise in clinical research, intellectual property strategy, and regulatory support.
What We Offer
Our subscription model is designed to adapt to your evolving needs, providing flexible, high-impact support across:
Clinical Research & Strategy:
Clinical trial design, study documentation preparation, study report preparation.
FDA submission preparation, including IDE and 510(k) documentation.
Data analysis, clinical site training, and ongoing study oversight.
Intellectual Property Development:
Patent ideation, drafting, and portfolio management.
Collaboration with legal teams to safeguard your innovations.
Regulatory & Medical Writing:
Creation of abstracts, reports, and regulatory submissions.
Guidance through pre-submission meetings and regulatory pathways.
Customized Advisory Services:
Regular strategy sessions to ensure alignment with business goals.
Expert insights into trends and innovations shaping the medical device landscape.
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:
Basic Tier: Ideal for early-stage support and advisory needs.
1-2 hours/month of advisor support
Document review and recommendations
Limited email support
Pricing: $1000 - $2000/month
Standard Tier: Comprehensive support for growing teams and active projects.
Bi-weekly strategy calls wi (Up to 4 hours/month of strategic support)
Document reviews and clinical/regulatory guidance
Assistance with regulatory submissions or IRB documentation
Collaboration with other team members
Pricing: $3000 - $5000/month
Premium Tier: Dedicated partnership for complex, high-stakes initiatives.
Weekly strategy calls (up to 8 hours/month)
End-to-End support for clinical trials, FDA submissions, or intellectual property portfolios.
Development of documents such as clinical study protocols, journal articles, breakthrough designations, etc.
Ongoing project management or collaboration with external stakeholders.