Bridging The Gap Between Development And Regulatory Teams

The mandatory nature of a regulatory-enabled process and the practical considerations of product design often create an undesirable tension between regulatory and development groups. 

The regulatory discipline needs a clear evolution of design inputs to design outputs with evidence and substantial justification. While developers may be prone to iterative solutions, which in turn, expose additional, nuanced needs. The intersection of these native tendencies creates a tension that can be counterproductive and obstructive to medical device development if not addressed. 

Register for this free, in-depth webinar presented by medical device expert Milton Yarberry, Director of Medical Programs at Integrated Computer Solutions, who will attempt a frank depiction of this collision of work practices, and focus on remedies in the form of processes, tools and approaches, that bridge the gap between development and regulatory.

Watch The Webinar

ICS-GG Webinar 6-16-22
Specifically, this webinar will cover:
  • Leveraging Prototyping
  • Single source of truth in requirements
  • Development Prerequisites
  • Managing change
Who Should Attend?
  • Software Developers
  • Regulatory Affairs Professionals and Management
  • Quality Professionals and Management
  • Medical Device Executives
Register Now  

Hosted by

MIlton (1)
Presenter: Milton Yarberry

Director of Medical Programs, ICS

Laura Court
Moderator: Laura Court

Medical Device Guru, Greenlight Guru

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About ICS

Integrated Computer Solutions' (ICS’) helps medtech innovators design medical devices, in-vitro diagnostics and SaMD that enhance usability and mitigate use error. We offer deep domain expertise, specialized tools, ISO 13485-compliant processes, and a tightly coupled suite of services to accelerate development, testing and certification. Applying IEC 62366, our software developers, HFE specialists, UX designers, and regulatory and cybersecurity experts create powerful solutions. And thanks to our experience with Agile processes, test-driven development and our own rapid-development approach, we reduce redundancies and costs, enhance software performance and compress the overall timeline of your next project. Visit their website to learn more.


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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