Life Science — Pharmaceutical SOP Validation Workflow

Overview

The Pharmaceutical SOP Validation Workflow is designed to ensure that newly created Standard Operating Procedures (SOPs) meet industry standards and regulatory requirements. The process begins with the ingestion of SOP documents from internal repositories. These documents are then sent to designated domain experts for validation, where their feedback is collected and integrated into a systematic review process. The workflow includes multiple processing steps: initial document submission, expert

The Pharmaceutical SOP Validation Workflow is designed to ensure that newly created Standard Operating Procedures (SOPs) meet industry standards and regulatory requirements. The process begins with the ingestion of SOP documents from internal repositories. These documents are then sent to designated domain experts for validation, where their feedback is collected and integrated into a systematic review process. The workflow includes multiple processing steps: initial document submission, expert review, feedback incorporation, compliance checks, and final publication. Quality controls are rigorously applied throughout, including regulatory compliance checks to ensure that all SOPs adhere to industry standards. Outputs of the workflow consist of validated SOPs, compliance reports, and a comprehensive library of published documents. Monitoring key performance indicators (KPIs) such as validation turnaround time and compliance rates allows for continuous improvement and operational transparency. This DAG not only enhances the reliability of SOPs but also significantly reduces the time required for validation, thereby increasing overall efficiency and compliance in life sciences operations.

Part of the SOPs & Playbooks solution for the Life Science industry.

Use cases

• Ensures compliance with industry regulations and standards
• Reduces time-to-approval for critical SOPs
• Enhances collaboration among subject matter experts
• Improves operational efficiency across life sciences teams
• Facilitates easy access to validated SOPs for stakeholders