Our Services
Tailored Medical Device Solutions – From Ideation to Implementation
Concept Development
Manufacturing Support
Quality Assurance
Design and Prototyping
Lifecycle Management
Regulatory Compliance
System Engineering
System Architecture & Requirement Definition
We translate clinical and product needs into clear system requirements and architectures. Our team ensures every subsystem aligns with medical safety, usability, and regulatory expectations.
System Integration
We integrate hardware, software, electronics, and mechanical components into a unified, reliable system. Our approach ensures smooth interoperability and stable device performance.
Risk & Safety Engineering
We apply medical device risk management practices to identify, assess, and mitigate potential hazards throughout the product lifecycle.
Verification & Validation Support
We create and execute structured verification, and validation plans to ensure your device meets technical, functional, and clinical requirements.
Hardware Engineering
Circuit & PCB Design
We design reliable electronic circuits and PCB layouts engineered for precision, safety, and manufacturability in medical devices
Component Selection & Optimization
We choose and validate components that meet performance, longevity, and regulatory requirements for clinical use
Sensor & Actuator Integration
Our team integrates sensors and actuators for accurate measurement, control, and feedback in medical systems
Prototype Development & Testing
We build and evaluate hardware prototypes to ensure electrical performance, robustness, and compatibility with the overall system
Mechanical Engineering
Mechanical Design & CAD Modelling
We develop 3D models and mechanical designs optimized for usability, durability, and medical safety
Industrial Design
Our team designs ergonomic, patient-safe enclosures that support proper device assembly, protection, and heat management
3D Printing & Moulding Solutions
We offer 3D printing services and molding support to help teams rapidly visualize concepts, evaluate form and fit, and create early prototypes. These solutions enable quick design iterations and accelerate the transition from concept to functional models
Prototype Development & Testing
We support rapid prototyping and design-for-manufacturing (DFM) to bring concepts closer to production readiness
Software Engineering
Embedded Software
Designs and develops low-levelfirmware for real-time operation, devicecontrol, sensor integration, andhardware interfacing in medical devices.
Cloud & Backend Systems
Develops scalable cloud infrastructure, APIs, and secure data pipelines to enable remote monitoring, analytics, and seamless device connectivity.
Mobile App Development
Builds intuitive, secure, and responsive iOS/Android applications for patient monitoring, clinician interaction, and real-time data visualization.
AI/ML Solutions for Innovation
We integrate advanced AI and machine learning solutions to enhance clinical decision-making, optimize device performance, and drive data-driven innovation across the MedTech ecosystem
UI/UX Design
User Research & Workflow Understanding
We study clinician and patient workflows to design interfaces that fit real medical environments
Wireframes & Interactive Prototypes
Our design team creates intuitive wireframes and prototypes that simplify interaction and reduce user errors
Human Factors & Usability
We incorporate human factors engineering to meet safety standards and enhance device usability
Visual Design & Interface Implementation
We deliver clean, accessible UI designs optimized for clarity, readability, and compliance with medical design principles
Regulatory Compliance
Standards & Compliance Alignment
We ensure product development aligns with relevant standards such as ISO 13485, IEC 60601, IEC 62304, and applicable clinical safety guidelines
Risk Management (ISO 14971)
Our team conducts hazard analysis, FMEA, and risk mitigation activities to ensure compliance with global safety requirements
Verification & Validation Documentation
We support the creation of V&V protocols, reports, and traceability to maintain complete regulatory alignment
Documentation
We prepare essential regulatory documentation including DHF, DMR, and technical files aligned with medical device standards
