Software solutions for medical devices

Our free white paper

ON CHALLENGES, INNOVATIONS AND SOLUTIONS IN THE DEVELOPMENT OF MEDICAL DEVICES

The overall market for digital products is constantly in flux – and this poses particular challenges for the development of medical devices. Extensive and regulatory requirements must be met without losing sight of the time to market. Opportunities arise from reusing software components, the use of cloud solutions and modern networking of the systems involved.

Read our free white paper to learn how software in medical devices must change to enable digitalisation and disruptive business models.

Based on our varied experience in the conception and development of software for medical devices, we will show you the concrete opportunities by means of an exemplary medical devices. With the help of the Interaction Room (IR), which serves as a catalyst for the successful implementation of your product, we work with you to develop a tailor-made solution.

Learn more about the following in our white paper...

  • … what challenges there are in the market.
  • … everything about the current challenges in the development of medical devices.
  • … what innovative solutions look like.
  • ... what the development of a virtual laboratory analysis device can look like, using a practical example.
  • … Wwhat opportunities and requirements there are from a regulatory perspective.
  • … how to proceed in concrete terms.

FREE WHITE PAPER: „INNOVATIVE SOFTWARE SOLUTIONS FOR THE MEDICAL DEVICES OF THE FUTURE“

REQUIREMENTS FOR THE SOFTWARE

Software plays a major role in more and more medical devices. Being an essential component of the medical devices, software has an influence on the time to market and generates additional risks in product development. There are special quality assurance measures in place for software. In addition, all regulatory requirements must be met. Learn how to master these challenges in our white paper.

Read our free white paper to learn how software in medical devices must change to enable digitalisation and disruptive business models.

OPPORTUNITIES AND REQUIREMENTS FROM A REGULATORY PERSPECTIVE

When developing software for medical devices, the regulatory requirements of the legislator must always be kept in mind. These can of course also have an impact on the IT solutions used.

From technical documentation to error analysis and evaluation, our white paper will show you how to meet these legal requirements and challenges in a legally compliant manner.

Do you have any questions?

Your contact person
Lars Schmiedeberg
Manager Life Sciences

No website or brochure can ever trump a face-to-face discussion about the goals and issues that are relevant to you. We look forward to meeting you at your site in person.

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