User's guide /

ProFlow Document Management

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General Information

Welcome to OBS ProFlow Document Management

The ProFlow Document Management system is an advanced, configurable solution designed to streamline and automate document workflows, particularly for industries with stringent regulatory requirements, such as pharmaceutical production.

Its core focus is on ensuring compliance with industry standards, improving operational efficiency, and providing full traceability of document versions and approvals through an integrated workflow process and automated notifications. 

Users are assigned specific roles, with clearly defined responsibilities for each stage of the document lifecycle. This role-based structure allows for seamless collaboration between departments while maintaining accountability at each approval stage.

From document upload through multi-step approvals to finalization, the system logs every action, creating a detailed audit trail that offers oversight for both internal reviews and external audits.

Key Features

  • Comprehensive role-based access control for secure document handling
  • Automated version control
  • Compliance with industry regulations
  • Flexible document revision management with approval workflows
  • Automated reminders and notifications for deadlines and approvals
  • Detailed audit trails for internal and external reviews

By automating key tasks and triggering reminders for upcoming reviews or required approvals, ProFlow reduces the likelihood of errors or missed deadlines, while ensuring that the entire process is highly auditable and traceable.

With an intuitive interface designed for ease of use, ProFlow enables users to quickly review, approve, and track documents, while tailoring workflows to suit specific business needs. This ensures that organizations remain compliant with regulatory frameworks, while maintaining an organized and efficient document management process.