HL7 FHIR Compliant Data Interoperability Cloud Architecture For IoMT & Medical Devices

HL7 FHIR Interoperability architecture to help IoMT, Wearable and Medical Device Companies create a DaaS and Cloud Intelligence platform with FHIR compliant APIs for data consumers.

ONC Data Interoperability Mandates in the US

To increase digital data interoperability between healthcare systems and data consumers such as CROs, Clinical Trials, Payors, Providers and Pharmaceutical companies, Office of the National Coordinator for Health Information Technology (ONC) has created following mandates:

Recent Government Announcements around Data Interoperability:

AIMDek’s Data Interoperability Cloud Architecture for IoMT & Medical Devices

With IoMT and Medical Device industry facing challenges due to the pricing concerns of consumers:

Sooner or later, to become a medical grade DaaS company or to create a Cloud Intelligence platform that shares or stream patient healthcare data to all their B2B data consumers such as CROs, Clinical Trial companies, Payors, Providers and Pharmaceutical companies, they would have to adhere to the HL7 FHIR interoperability mandates!

Introducing Medical Grade DaaS Accelerator Architecture for Cloud

Supported Cloud System

The Architecture

IoMT Streaming Devices

This architecture is defined to transmit any sort of data from edge devices to the cloud.

Data Management Architecture

We ensure that your data is stored securely and that it is HIPAA compliant.

Data Storage

A multi-layer storage facility that helps in cost-optimization for short-term associations and long-term storage.

HL7 FHIR Compliant Processing

A state-of-art data syntactic and semantic parser, classifier, and distribution model that decouple the data filter it into a completely dynamic data set that can be paired and connected on demand.

Post-processing HIPAA-compliant Storage

Post processing the data is stored in a secure and meaningful manner in an elegant database that is completely secure, dynamic, scalable, and HIPAA compliant.

ONC mandate friendly distribution APIs infrastructure

Once the data is processed, it can be delivered in bulk or in near-time streaming to CROs, Clinical Trials, Healthcare Payors, Healthcare Providers, and any other potential data consumers as ready-to-use APIs that are built as per the guidelines set by the Interoperability and Patient Access final rule (CMS-9115-F).

Benefits

Premarket Medical Device Cybersecurity Readiness Services

Ensure your medical devices’ readiness for the US market and get FDA 510(k) cybersecurity approval with AIMDek’s premarket Medical Device cybersecurity readiness services.

We deploy a team of subject matter experts that help you understand the process and provide detailed cybersecurity and software security testing services to ensure 510(k) readiness with minimal efforts from your end.

As a part of our comprehensive cybersecurity assessment services, we provide our clients with:

LOOKING TO CONVERT FROM CONSUMER TO MEDICAL GRADE DEVICE ?

Wish to employ our AIMDek DaaS Accelerator?

TALK TO OUR SUBJECT MATTER EXPERT