Customer – demand – driven, leveraging interdisciplinary collaborative innovation to develop compliant and reliable medical device product design solutions.
01
Concept Analysis
Requirement Communication
Product Design
Product Feasibility Analysis
Patent Analysis
Rapid Prototyping
02
Prototype Development
Detailed Product Design
Test Method Development
Design Validation/Verification
Prototype /Sample
Risk Management
03
Design for Manufacturability
Material Research
Structural Design Optimization
Manufacturing Process
Mold Trial Verification
Lean Methods/Tools
We specialize in innovative design and efficient development of medical devices
Our cross-functional team works closely with customers through a rigorous multi-stage design process, we ensure precise control over every step of a product’s journey, from initial concept to market launch. We are committed to adopting using industry leading technologies and tools to create safe, reliable and cost-effective medical solutions, while strictly verifying the entire development process— starting from research and development stage to series production.
We encourage with transparent communication, detailed documentation and continuously optimized production plans to provide customers with seamless industrialization support and fully cooperate in the launch of innovative products while meeting global market standards.
Active Device Design and Manufacturing
We offer flexible collaboration models covering the entire technology productuots for clients, including medical device companies, startups, and healthcare institutions.
01
Product Requirements
-Collaborate with medical
institutions to identify clarify user pain points, technical analysis and product definition.
02
R&D Design
-System structure – Software framework design -Human factors engineering research
03
Software Development
-Embedded development -Supporting software development
04
Hardware Development
-Circuit design -Engineering prototypes.
05
Mechanical Development
-Industrial design -Structural design
06
Clinical Trials
-Compliance preparation -Trial protocols
07
Regulatory Registration
-Technical documentation and system dicuments -FDA/CE/NMPA registration