Life Science — Multi-Source Data Ingestion for Regulatory Research

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This DAG facilitates the ingestion of multi-source data for regulatory research in life sciences. It ensures data quality and compliance through normalization and role-based access controls.

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Overview

The purpose of this DAG is to streamline the ingestion of diverse data sources essential for regulatory research in the life sciences sector. It collects data from various systems, including ERP systems, CRM databases, and shared documents, ensuring a comprehensive view of the information landscape. The ingestion pipeline begins with the extraction of data from these sources, followed by a rigorous normalization process that standardizes the data formats to enhance consistency and reliability. T

The purpose of this DAG is to streamline the ingestion of diverse data sources essential for regulatory research in the life sciences sector. It collects data from various systems, including ERP systems, CRM databases, and shared documents, ensuring a comprehensive view of the information landscape. The ingestion pipeline begins with the extraction of data from these sources, followed by a rigorous normalization process that standardizes the data formats to enhance consistency and reliability. This is crucial for maintaining data quality and ensuring compliance with industry regulations. Additionally, historical data is preserved to facilitate audits and traceability. Role-Based Access Control (RBAC) is implemented to secure data access, allowing only authorized personnel to view sensitive information. The processed data is then cataloged for easy retrieval and is stored in a centralized data warehouse, which serves as a foundation for further analysis and reporting. Key performance indicators (KPIs) such as data ingestion speed, error rates, and compliance checks are monitored to ensure the ongoing effectiveness of the pipeline. The business value of this DAG lies in its ability to provide quick, reliable access to critical data, thereby supporting informed decision-making and enhancing regulatory compliance in life sciences research.

Part of the Knowledge Portal & Ontologies solution for the Life Science industry.

Use cases

  • Improved regulatory compliance through standardized data
  • Enhanced decision-making with reliable data access
  • Increased efficiency in data management processes
  • Streamlined audits with preserved historical data
  • Secure data sharing among authorized personnel

Technical Specifications

Inputs

  • ERP transaction logs
  • CRM customer interaction data
  • Shared regulatory documents
  • Clinical trial data
  • Market research reports

Outputs

  • Normalized data sets for analysis
  • Comprehensive data catalog
  • Access logs for compliance audits
  • Data quality reports
  • Centralized data warehouse

Processing Steps

  1. 1. Extract data from ERP, CRM, and shared documents
  2. 2. Normalize data formats for consistency
  3. 3. Preserve historical data for compliance
  4. 4. Implement role-based access controls
  5. 5. Catalog processed data for easy retrieval
  6. 6. Store data in a centralized warehouse
  7. 7. Monitor KPIs for ingestion performance

Additional Information

DAG ID

WK-1421

Last Updated

2026-01-10

Downloads

64

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