Data Integration for Medical Device Manufacturing

Connect QMS, MES, and regulatory systems with validated data pipelines. Maintain FDA 21 CFR Part 11 compliance while accelerating time-to-market.

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Industry-Specific Outcomes

QMS to MES integration for quality monitoring

Clinical trial data consolidation for regulatory submissions

End-to-end supply chain traceability and UDI compliance

Post-market surveillance data aggregation and analysis

Manufacturing equipment IoT data for predictive maintenance

Data engineering resources

Popular Connector Workflows

Source System

Destination

Use Case

PostgreSQL

Snowflake

QMS quality records to analytics warehouse

MySQL

BigQuery

MES production data for manufacturing dashboards

Salesforce

Snowflake

Clinical trial data for regulatory reporting

Oracle

Databricks

ERP supply chain data for traceability

Amazon S3

Snowflake

IoT sensor logs for predictive maintenance

Medical Device Data Pipeline Architecture

Validated pipelines connecting QMS, MES, PLM, and regulatory systems to centralized analytics platforms with audit trails.

Our business deals with a lot of PII data, and we didn't want to waste hours trying to find out where and how third-party solutions are storing our data. With Airbyte, we could just push a few buttons, allow API access, and bring all the data into Google BigQuery. Now, we can easily tell how any customer entered our platform, how much they cost, and their ROI.