Life Science — Research and Development Compliance Monitoring Pipeline

Free

This DAG monitors R&D processes to ensure regulatory compliance in life sciences. It collects metrics, generates audit reports, and triggers alerts for detected anomalies.

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Overview

The purpose of this DAG is to monitor research and development processes within the life sciences sector to ensure adherence to regulatory compliance standards. By integrating various data sources, it collects essential metrics related to R&D activities. The ingestion pipeline begins with the extraction of data from laboratory information management systems (LIMS), clinical trial management systems (CTMS), and regulatory submission databases. These inputs are processed through a series of transf

The purpose of this DAG is to monitor research and development processes within the life sciences sector to ensure adherence to regulatory compliance standards. By integrating various data sources, it collects essential metrics related to R&D activities. The ingestion pipeline begins with the extraction of data from laboratory information management systems (LIMS), clinical trial management systems (CTMS), and regulatory submission databases. These inputs are processed through a series of transformation steps, including data validation, anomaly detection, and compliance checks. The processing logic applies machine learning algorithms to identify deviations from expected performance metrics and regulatory standards. Quality controls are implemented at each stage to ensure data integrity and accuracy. The outputs of this DAG include comprehensive audit reports, compliance status dashboards, and alert notifications for any detected anomalies. Monitoring key performance indicators (KPIs) such as alert response time and compliance rates provides insights into operational efficiency and regulatory adherence. This DAG delivers significant business value by enhancing compliance oversight, reducing risks associated with non-compliance, and improving the overall quality of R&D processes in the life sciences industry.

Part of the Scientific ML & Discovery solution for the Life Science industry.

Use cases

  • Ensures adherence to strict regulatory standards
  • Reduces risk of non-compliance penalties and fines
  • Improves operational efficiency in R&D processes
  • Enhances data-driven decision-making capabilities
  • Facilitates timely responses to compliance issues

Technical Specifications

Inputs

  • Laboratory Information Management System (LIMS) data
  • Clinical Trial Management System (CTMS) logs
  • Regulatory submission databases
  • Research project tracking spreadsheets
  • Quality control test results

Outputs

  • Comprehensive audit reports
  • Compliance status dashboards
  • Alert notifications for anomalies
  • Performance metric summaries
  • Regulatory compliance certificates

Processing Steps

  1. 1. Extract data from LIMS and CTMS
  2. 2. Validate data for accuracy and completeness
  3. 3. Detect anomalies in R&D metrics
  4. 4. Perform compliance checks against standards
  5. 5. Generate audit reports and dashboards
  6. 6. Send alert notifications for detected anomalies
  7. 7. Monitor KPIs for continuous improvement

Additional Information

DAG ID

WK-1358

Last Updated

2026-02-15

Downloads

24

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