Medical device professionals know they must follow specific regulations — some of them even know what those regulations are. But how many professionals know how those regulations can help them be better designers and make their companies stronger?
In this webinar, the featured speaker will discuss some of the best practices for Design Controls and about truly understanding the reason for building a device. The speaker will discuss how to use that information to streamline the process from User Needs to Validation. Also, there will be a discussion about how to use design controls to mitigate risks within a product that might have not been previously recognized.
Speaker
Etienne Nichols, Community Manager and Medical Device Guru, Greenlight Guru
Etienne Nichols is a Medical Device Guru and Mechanical Engineer who loves learning and teaching how systems work together. He has both manufacturing and product development experience, even aiding in the development of combination drug-delivery devices, from startup to Fortune 500 companies and holds a Project Management Professional (PMP) certification. His expansive knowledge, experience, and passion with medical devices is evenly matched with how much he enjoys helping customers work efficiently through the design and development process to bring safe, high quality products to market.
Message PresenterWho Should Attend?
- Medical Device Industry Executives
- Quality Professionals and Management
- Regulatory Professionals and Management
- Clinical Affairs Professionals and Management
- R&D Engineers and Management
What You Will Learn
After this webinar, you will be able to:
- Better articulate the User Needs of devices
- Translate the newly discovered User Needs into better Design Inputs
- Use design controls to mitigate risk within a product
Xtalks Partner
Greenlight Guru
Greenlight Guru is the only all-in-one medical device success platform helping solve the unique challenges of device makers across their entire product’s lifecycle. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance, and provides a single source of truth by connecting the management of quality, product development, and regulatory processes. Greenlight Guru’s platform is used by over 500 medical device companies across the globe to push beyond baseline compliance and achieve True Quality for their devices. For more information, visit http://www.greenlight.guru.
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