Offerings
Transforming product ideas into Reality. Our experts work closely with Customer teams to provide services from Ideation to Finished Product and more under ONE roof
Transforming product ideas into Reality. Our experts work closely with Customer teams to provide services from Ideation to Finished Product and more under ONE roof
FPGA/ASIC Design Support
State of the art PCB Design
Efficient Circuit Design including choice of processors, connectivity protocols, efficient data flow etc
Support for 3rd party certification requirements GDPR, Cybersecurity Adherence, HIPAA Compliance, FDA, CE, DEKRA
Infrastructure and Lab for board bring up and functional validation of proto types and low volumes
Software development and documentation in line with industry standards
Platform based firmware development for a plug and play architecture
Responsive and Touch enabled Web UI Development
Native and Hybrid Applications development for iOS and Android
Software development and documentation in line with industry standards
State of the art test methodologies, manual and automated with well-defined test reports
In house Quality Assurance Systems in accordance with ISO 13485 and IEC 62304
Structural Design, User Experience Design
UX/UI design for web and apps
Scalable, Multi tenanted architecture
Targeted for most B2B IoT Application Scenarios
Licensable, in-house Java based platform iOrbit Health System, Internet of Medical Things
Enable Edge Compute for higher functional performance
Range of deployment methodologies to suit various regulatory and performance requirements
The regulations process surrounding medical devices involves a strict adherence to regulatory compliance throughout a device’s life-cycle. Medical devices, healthcare cloud platforms and services are expected to be compliant with the applicable regulations and laws. Data privacy and data security related to sensitive patient information is of utmost importance. Even a single compliance issue can have a significant effect on business. For every end- to-end medical device development project, we apply an arduously thought-through Regulatory strategy and homologation plans to get the right submissions for timely certification from Regulatory bodies.
Our ‘Design For Safety’ and ‘Design For Security’ approach always bear the “Patient first” criteria to make the products very safe, secure and reliable.
Our dedicated team of regulatory experts ensure that each product we offer or the project we undertake, is meticulously assessed, tested, and documented to meet the stringent demands of various international regulatory authorities. From initial concept to final delivery, we employ a holistic approach to regulatory activities.