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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Training Management CAPA Management Audit Management Product Development

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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Accelerate development with integrated design control and risk software.

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Featured Capabilities:

Design Controls Risk Management Risk Intelligence

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys Product Add-Ons

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FREE ON-DEMAND WEBINAR

Why User Needs Matter & Their Benefits in Streamlining Device Design and Development

Have you ever been caught up in the minutiae of bringing a device to market that you lost sight of who you were designing your product for in the first place?

Developing a safe and effective medical device involves more than just considering quality and regulatory requirements at the outset of design planning. The product should also fit into a real-life scenario and meet every stakeholders’ expectations, specifically the end user.

By having a firm understanding of who will use your device and why they will use it, you can seamlessly design the proper inputs and streamline processes to get to market.

Watch the webinar
Why UN matter webinar
Specifically, this webinar will cover:
  • What user needs are and why they matter
  • The role of user needs during design and development
  • An intersection approach: ideas to uncover all stakeholder needs
  • How to uncover all stakeholder needs using an intersection approach
  • Design metrics that meet regulatory requirements
  • Q&A Session
Who Should Attend?
  • Medical Device Executives
  • Product Development Engineers
  • Product Managers
  • Regulatory Affairs Professionals
  • UX Designers
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Hosted by

PK--Novo
Presenter: Philippe Kamdem

VP of Strategy, Novo
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Moderator: Jon Speer

Founder & VP QA/RA, Greenlight Guru

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About NOVO

NOVO is a strategic product design and innovation company. Our integrated services feature product strategy, industrial and UX design, electronic and mechanical engineering, and firmware & software development. Our services and approach provide substantial product design and development experience, as well as technical, financial and market benefits.

For our global clients in the medical industry, we deliver best-in-class product design and development strategy. We’ve supported a range of medical products including cardiovascular devices, digital health systems, ophthalmology tools, optics, respiratory devices, and patient-monitoring systems. Our Health Canada and FDA/compliance support, all driven by our solid engineering processes, help companies achieve higher product quality and accelerate time to market. Visit Novo's website to learn more.

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About Greenlight Guru

Greenlight Guru is the only Medical Device Success Platform (MDSP) for companies to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based software, Greenlight Guru is easier to implement, easier to use and designed to fit all medical device needs to enable innovative, safe and effective, True Quality medical devices. Visit our homepage to learn more.

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