Overview
Triple Ring provides a broad range of technical product development capabilities, from requirements definition to manufacturing support. Through appropriate upfront analysis, modeling, and MCAD capabilities, we take the surprise out of prototype and product development. Our electronic circuit design, simulation and testing capabilities include analog, digital, and mixed-signal PCBs; CPLDs and FPGAs; and mixed-signal ASICs. We have extensive experience with the design of optical systems, devices, and packaging. Our mechanical design and prototyping expertise includes designs for low volume or high volume production, DFM, DFA, CAD layout and piece-part design; material selection; thermal, stress, and tolerance analysis; parts and assembly documentation; and prototype fabrication. We provide software development for complex embedded medical systems, signal processing, networking, and end-user applications.
Triple Ring’s rich experience in product development includes several first-to-market devices that range from the very small (microfabricated sensors) to the very large (CT imaging systems) and embody simple but clever design solutions to highly sophisticated electro-optomechanical systems. Triple Ring tailors resources to the needs of our clients' projects. We can address the full range of project requirements - from initial feasibility assessment through detailed implementation and pilot production. When an organization needs to investigate technologies and products outside their technical competency, Triple Ring can help. Our experts can supplement an existing team, or provide expertise not already on staff to accelerate critical projects and help meet key deadlines.
“We often face complex interdisciplinary development challenges. The Triple Ring team brings
extensive scientific background and technological expertise to quickly and effectively extend the
capabilities of our own technical staff.”
David Shack
Director of Hardware Engineering
Fortune 500 Medical Device and Instrumentation Company
Our services include:
Definition
Triple Ring’s engineers will guide you through a systems approach to clarifying your product vision. This process results in a well-defined path for realizing a product concept; provides focus on the high-risk technical, market, and regulatory challenges; and enables rapid development of proof-of- concept prototypes.
Product Definition and Analysis
- System architecture definition
- Modeling and simulation
- Product and Project risk analysis
- Tools: MathCad, MATLAB
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Design
Triple Ring’s process embodies a disciplined, data-driven approach to design, enabling our engineers to retire risks and efficiently converge on solutions to key design challenges and human factors considerations.
Electrical, Optical, Mechanical, and Software Engineering
- Desktop applications to complex embedded systems
- Mission-critical applications
- Analog, digital, mixed-signal design
- High-speed data acquisition and processing
- MPPA and FPGA programming
- Tools: Orcad, Allegro, PADS, Zemax, TracePro
- Mechanism and package design
- Low to high-volume plastic and metal component design
- Tools: Solidworks, Pro-E, Mechanica
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Development
Whether a new product development program, a redesign for cost reduction or, DFM/A and reliability, Triple Ring ensures product cost and performance targets are met through product design for ease of assembly and high yield manufacturing processes.
Systems Engineering
- Human factors and industrial design
- Verification and validation
- Packaging and sterilization
- Statistics and data analysis
- ISO 13485-compliant quality system
- Regulatory strategy and certifications
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Testing
Years of experience with medical devices brings an appreciation of the need for thorough design testing. We provide testing services that include test procedure creation and documentation, test tool creation, design verification and validation (including requirements traceability), DOE and data analysis, EMC/EMI testing, and environmental testing.
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Regulatory Compliance
Regulatory compliance is an important part of the development process. Considering regulatory requirements early in the development process can help avoid expensive, time consuming steps later on. Triple Ring can provide regulatory support and guidance through every stage of the process. We can provide a liaison to the FDA; generate 510(k), PMA and IDE submittals; and assist in establishment registration, device listing, initial and annual reports, and variances. We also conduct QSR/cGMP compliance audits and help establish device master records. We offer support for FDA inspections, response to FDA 483 observation reports and warning letters, medical device reporting (MDR), and recalls. Triple Ring can also help your organization with user labeling and field service documentation; product, equipment, and process validation; and UL/IEC compliance
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Dedicated On-site Consultants
Some client projects require full-time resources to be integrated on-site into their development teams for a specific project. Triple Ring's team is available to work on-site with clients on these critical projects.
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