Prepare a SOP on document control

Version 1 - Last updated 23rd July 2025

When prepared the standard operating procedure (SOP) should address the following points:

Access (protection and retrieval)

  • Define access levels:
    • View only for general staff.
    • Edit/upload for authorised personnel, such as chemical responsible team or person.
  • Designate a central authority to control all documents (preferably the Chemical Responsible Person/Team).
  • Describe the workflow and procedures for managing chemical management system-related documents.

Location (retention)

  • Ensure easy access for relevant staff.
  • General documents (e.g., SDS or chemical policy) should be available to all staff.
  • Department-specific documents (e.g., training records for HR, brand RSL documents for QC lab) should be accessible to relevant departments.
  • Store documents as:
    • Hard copies in files.
    • Soft copies on the company server or open-source platforms (e.g., Google Drive).
  • Assign access permissions for "view only" or "view and edit".
  • Communicate the location(s) of all documents and records to the staff.

Review (updates and removal)

  • Implement a regular review process.
  • Update obsolete documents with new ones.
  • Delete or destroy documents that are no longer valid.

Following is a template which can be used to maintain a summary of revisions made in the chemical management system:

Download document control revision template