<img src="https://ws.zoominfo.com/pixel/OJkQgdjSvoid2NFoB5Qs" width="1" height="1" style="display: none;">
 
Free On-Demand webinar

5 Key Points to Consider in Design Transfer of Medtech

Watch the webinar


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.

 

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

Presenter

doug-browne

Doug Browne
Director of Mechanical Engineering & Design Transfer
Sunrise Labs

tedTrask Round

Ted Trask
Director of Corporate QA/RA
Cirtronics

Moderator

 Jesseca round

Jesseca Lyons
Operations and Enablement Guru
Greenlight Guru

     

 
sunrise
 
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.

 

Cirtronics_logo

 
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.

 

 

greenlight-guru-logo
 
About greenlight guru

Greenlight Guru is a modern quality management software platform used by medical device companies in over 25 countries to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based eQMS, Greenlight Guru is easier to implement, easier to use and simply fits medical device processes out-of-the-box allowing companies to innovate faster and be more efficient.

Visit our homepage to learn more.

 

 

FEATURED IN