Business Details
29 Years
experience
Engineering, Design & Low-Volume Manufacturing Experts
Founded in 1997, our firm employs an interdisciplinary approach combining engineering expertise with innovative industrial design to solve complex product development challenges. We specialize in medical device development, robotics, and low-volume manufacturing, maintaining ISO 13485 certification to ensure compliance with stringent quality standards. Our on-site partnership model places experienced engineers directly with client teams, backed by our full organizational resources. With over 25 years of experience and a 95% repeat business rate, we prioritize client success through technical precision, regulatory compliance, and client-owned intellectual property. Our commitment to quality extends across all operations, balancing speed with safety in life-critical applications while maintaining transparency and accountability in every client relationship.
Services
Medical Device Development
Robotics & Automation
Low-Volume Manufacturing
Human Factors Engineering
Industrial Design
Product Development
Medical Device Regulations
Medical Device Design
Prototyping
On-Site Engineering Services
Served areas
- Maine, New Hampshire, Massachusetts, New York, Rhode Island, Connecticut, Vermont
Details
- Year established: 1997
Highlights and features
- ISO 13485 certified with 25+ years of medical device development expertise
- On-site partnership model combines individual engineers with full team support
- Interdisciplinary teams handle all phases from prototyping to manufacturing
- Client-owned intellectual property generation during all development projects
- 95% repeat business rate demonstrating long-term client satisfaction
Associations and certifications
- ISO 13485:2016
Services
Medical Device Development
Our interdisciplinary teams guide medical technology from concept to commercialization while maintaining FDA compliance. With ISO 13485 certification and 25+ years of experience, we handle all development phases from initial design through regulatory submission. Our approach prioritizes patient-centered design while ensuring technical precision in life-critical applications.
Low-Volume Manufacturing
We bridge prototyping and full-scale production with pilot line setup and process validation. Our services include quality control systems implementation, fixture development, and manufacturing documentation management. This transitional approach reduces investment risk while enabling design optimization before large-scale production commitments.
Robotics & Industrial Automation
Our engineering experts create customized robotic solutions from surgical systems to industrial automation. We maintain safety standards while addressing complex technical requirements through flexible, interdisciplinary teams. Our approach ensures tailored solutions that adapt to specific application needs and industry regulations.
Human Factors Engineering
We integrate human-centered design principles throughout product development cycles. Our approach combines usability testing with regulatory compliance requirements, particularly in medical applications. By focusing on user needs, we create intuitive interfaces that enhance product effectiveness and safety in real-world environments.
On-Site Engineering Services
Our unique partnership model places engineers directly at client locations while maintaining organizational support. This approach combines individual expertise with collective resources for greater problem-solving capability. We provide temporary staff augmentation to complete engineering teams during critical development phases.
Questions
What industries does Goddard Technologies, Inc. specialize in?
We primarily serve medical device development, robotics, and industrial automation sectors while also supporting consumer product development. Our expertise spans both regulated medical environments and complex technical challenges across multiple industries.
Are Goddard Technologies, Inc.'s engineers ISO 13485 certified?
Yes, our company maintains ISO 13485 certification for medical device development. This ensures our processes meet international quality management standards specifically for medical technology applications.
How does Goddard Technologies, Inc. handle regulatory compliance?
We specialize in FDA-regulated medical device development and maintain established quality systems for compliance. Our team understands regulatory requirements and implements them throughout the product development lifecycle.
Can Goddard Technologies, Inc. help with complete product development cycles?
Yes, we support all phases from concept through commercialization. Our services include design engineering, prototyping, regulatory submission preparation, and transitional manufacturing support for complex technical products.
What is Goddard Technologies, Inc.'s approach to intellectual property?
All intellectual property created during projects is 100% client-owned. We ensure our development work directly benefits our clients without creating ownership barriers for their products or technologies.
Do you provide on-site engineering support?
Yes, our partnership model includes placing engineers directly at client sites while maintaining full organizational support. This enables seamless collaboration with client teams while accessing our complete resource network.
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