Life Science — SOP and Playbook Update Automation

Overview

The purpose of this DAG is to manage the timely update of Standard Operating Procedures (SOPs) and playbooks in the life sciences sector by integrating the latest regulatory and scientific information. The architecture of the DAG consists of a data ingestion pipeline that pulls in various data sources, including regulatory updates, scientific research publications, and internal compliance reports. The first step involves ingesting these data sources, followed by a transformation process where th

The purpose of this DAG is to manage the timely update of Standard Operating Procedures (SOPs) and playbooks in the life sciences sector by integrating the latest regulatory and scientific information. The architecture of the DAG consists of a data ingestion pipeline that pulls in various data sources, including regulatory updates, scientific research publications, and internal compliance reports. The first step involves ingesting these data sources, followed by a transformation process where the information is analyzed for relevance and compliance. Each document is then subjected to a quality control check to ensure it meets the required standards before publication. Key performance indicators (KPIs) for this process include the update turnaround time and the compliance rate of the documents. In the event of discrepancies or issues identified during the quality control phase, a revision process is triggered to address the concerns. The outputs of this DAG are updated SOPs and playbooks that are ready for distribution across the organization. Monitoring tools are in place to track the efficiency of the update process and ensure adherence to regulatory requirements. The business value of this automation lies in reducing manual effort, minimizing compliance risks, and ensuring that all operational documents are current and reflective of the latest industry standards.

Part of the Document Automation solution for the Life Science industry.

Use cases

• Increased operational efficiency through automation
• Enhanced compliance with regulatory standards
• Reduced risk of outdated procedures and protocols
• Faster response to changes in regulations
• Improved collaboration across departments with updated documents