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The
Reports
R&D Reports for Medical Device Innovators
Make smarter, faster decisions with detailed development plans modeled on real-world devices. Whether you're validating an idea or preparing to raise capital, these reports break down the cost, timeline, and complexity of bringing a device to market.
Beyond the Numbers — Your Development Roadmap
Zewski Reports are built with one core philosophy: every concept deserves to be treated like an original invention. That means each report starts from a clean slate — assuming your product doesn’t yet exist, and that it needs to be developed from idea to market.
1. The Product Exists Only as an Idea
Each report assumes your device is in its earliest conceptual stage, requiring full development — including human factors, design, engineering, prototyping, testing, regulatory planning, and manufacturing setup. Even if similar products already exist, we approach the process as if you're building a new category.
2. The Device Does Not Yet Exist
We treat your idea as if it’s being introduced to the world for the very first time. This gives you a realistic picture of:
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- The development effort
- The regulatory and technical challenges
- The market risks and resource needs involved in building something truly novel
Not Meant for “Me Too” Products
These reports are not designed for cloning existing solutions. They don’t model the cost of copying — they model the challenge of creating. That’s what makes them powerful for:
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- Strategic planning
- Investor readiness
- Understanding what it takes to innovate in today’s market
Each report is designed to help you plan confidently — here’s what you can expect.
What are these reports based on?
Based on our original R&D calculator, each report is tailored to a specific medical device type and grounded in real-world development scenarios. We apply modeled assumptions that reflect actual engineering, testing, and regulatory pathways — including phase-specific milestones, risk considerations, and cost drivers. This approach ensures that the guidance in each report isn’t just theoretical — it mirrors what real inventors encounter as they move from concept to commercialization.
What do I get in each report?
Each report delivers a comprehensive, device-specific roadmap that spans the full development journey. You’ll receive customized insights on projected cost and timeline ranges, based on the device’s complexity and technical features. The report outlines the likely regulatory pathway, identifies key market dynamics, and breaks the process into clearly defined development phases. It also includes guidance on assembling the right team, allocating resources efficiently, mitigating development and compliance risks, and preparing for investment or commercialization — all grounded in your actual product concept.
Who are these for?
These reports are designed for inventors, entrepreneurs, and early-stage teams who are navigating the complex process of bringing a medical device to market. Whether you're developing your first proof-of-concept, preparing for regulatory submission, or exploring the business potential of a new idea, these reports provide the clarity and structure needed to move forward confidently. They’re especially valuable for individuals or small teams without full in-house regulatory or engineering support — offering practical, product-specific guidance that helps bridge the gap between concept and commercialization.
Can I preview the report before buying?
The first few sections of the report are fully visible so you can see the writing style, level of detail, and how the information is structured — this way, you can confidently assess the value before committing. The remaining sections with deeper technical and strategic insights are behind a paywall, but you’ll get instant access to the full report immediately after purchase.
How are these different from templates or whitepapers?
These reports are detailed, structured, and built to support real-world decision-making. They offer targeted insights tailored to each device — guiding inventors through development, testing, and regulatory planning with clarity and purpose.
