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From Concept to Market‑Ready Medical Device

From professional defibrillators to the world’s smallest AED, Corscience has decades of experience delivering safe and reliable medical device development.

Using a systems‑level approach, we support your projects from the initial concept through regulatory approval. Our broad expertise in system engineering, combined with proven technology building blocks, accelerates development and helps minimize potential risks.

With deep experience in safety‑critical systems – from defibrillation and monitoring to ventilation – and strong regulatory expertise, we serve as your single point of contact for development, approval, and production.

Whether it involves patient safety, user safety, electrical safety, or functional safety: Safety is always part of the design at Corscience.

Our Approach to Medical Device Development

Understand & Focus

In this early phase, we dive deep into the product vision, application context, and requirements. Through workshops and creative sessions, we refine the system footprint, define the USP and product goals, and develop a solid initial understanding.

With intensive brainstorming and structured thinking, we help our customers specify their idea and establish the right focus.

Plan & Structure

We set up the joint project, clarify roles, responsibilities, regulatory frameworks, and the complete project and QA plan. At the same time, the concept phase produces the system architecture, supported by feasibility studies, technical analyses, and the detailed definition of requirements.

This turns the initial vision into a clearly structured, well‑thought‑out project plan — including first test concepts and a well‑defined scope

Develop & Validate

During the functional prototype phase, the first complete device design is created: hardware, software, and mechanics are developed, integrated, and validated in early tests. Building on this, we create prototypes with final mechanics, final hardware, and tested software.

At the end of this phase, you receive a near‑production‑ready device with fully verified and documented functionality.

Qualification & Transfer

Independent system tests, external assessments (e.g., EMC, notified bodies), and targeted bug fixing ensure full qualification of the product. We then support the smooth transfer to production, coordinate with manufacturing partners, and assist with pilot series and industrialization.

The result: a fully qualified, manufacturable medical device — clearly documented and ready for production.

Life-Cycle-Management

After market entry, we support you throughout the entire product lifecycle: from maintenance and further development to updates and variants, all the way to compliance adjustments and obsolescence management.

This ensures your product remains safe, compliant, and successful in the long run.

In addition to full‑scale development, we also support you in specific areas of MedTech development

Whether you need targeted consulting, specialized expertise, or the execution of clearly defined work packages – we step in exactly where you need us and seamlessly complement your teams.

 

Are you looking to turn an idea into a product?

 

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