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Greenlight Guru QMS

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

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Featured Capabilities:

Document Management Product Development Design Control Risk Solutions Training Management CAPA Management

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

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SMART-TRIAL by
Greenlight Guru

Data gathering and management designed for MedTech clinical trials and operations.

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Featured Capabilities:

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

Get a personalized demo of SMART-TRIAL by Greenlight Guru today.

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Greenlight Guru Academy

Learn valuable, career-boosting skills for the Medical Device industry. Get access to hundreds of free resources as well as subscription-based courses and certifications.

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Discover the new trends, outlooks, challenges, and opportunities in the MedTech industry in 2023.

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FREE ON-DEMAND WEBINAR

5 Key Points to Consider in Design Transfer of Medtech

Design Transfer is often viewed as a one-time event. However, it should be an integral and ongoing part of the product development process, and should begin as early as possible. 

Communication between collaborators (“The Team”) is crucial to turning innovative ideas into commercial medical devices. The Team must identify and maintain procedures and checkpoints that ensure the design requirements successfully translate into production processes and specifications. 

This includes designing and specifying final test procedures and performance required for acceptance. Through early collaboration, seamless transfer to manufacturing is possible; increasing production efficiency, improving yield, decreasing re-work and shortening time-to-market.

During this informative presentation, Doug Browne, Director of Mechanical Engineering and Design Transfer at Sunrise Labs, and Ted Trask, Director of Corporate Quality Assurance/Regulatory Affairs at Cirtronics will share tips from their decades of real-world experience. They will discuss critical moments in the development journey where collaboration and communication lead to successful transfer of new medical products to full scale manufacturing.

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Specifically, this webinar will cover:
  • Building successful relationships throughout the product design process 
  • Identifying and mitigating risks early 
  • DFx optimization including manufacturing, testability, serviceability and sustainability 
  • Creating a supply chain strategy based on BOM, scalability, and fluctuations
  • The power of focusing on your strengths and working with trusted partners
Who Should Attend?
  • Project and Product Managers
  • Supply Chain and Operations Professionals and Management
  • Medical Device Executives
  • Regulatory Affairs Professionals and Management
  • Quality Professionals and Management
  • R&D Engineers and Management
 Register Now

Hosted by

doug-browne
Presenter: Doug Browne

Director of Mechanical Engineering & Design Transfer, Sunrise Labs
tedTrask Round
Presenter: Ted Trask

Director of Corporate QA/RA, Cirtronics
Jesseca round
Moderator: Jesseca Lyons

Operations and Enablement Guru, Greenlight Guru

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About Sunrise Labs

For almost 30 years, clients have come to Sunrise Labs for complete product development and engineering services, leveraging our ISO 13485:2016 certified process. We are known for solving tough engineering problems and turning novel ideas into commercially viable products. Client success stories reflect our strength in developing devices ranging from wearable, ultra-low power, wireless patient monitoring devices, through complex electro-mechanical Class III medical products.
Our portfolio spans patient monitoring solutions, imaging, cardiac, therapeutic, dermatology, neuro, IVD, combination products and connected system applications. Sunrise Labs brings expertise in User Research, Interaction Design, Human Factors, Full Stack Software, Analog and Digital Electronics, Systems, Mechanical and Optical engineering to each client challenge. Visit their website to learn more.

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About Cirtronics
Cirtronics is a contract manufacturer in the greater Boston area. They excel at manufacturing to meet the exacting standards of medical devices, medical lab equipment, robotics and other quality-intensive, regulated industries. Cirtronics is experienced in optimizing and validating DFM.
They have a Transition to Manufacturing center which includes collaborative pre-production builds alongside customer engineers, expert supply chain strategy, and complete build documentation. Their comprehensive T2M services accelerate program transfer into full scale manufacturing. Cirtronics is ISO 9001 and ISO 13485 Certified, and FDA Registered. Visit their 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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