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SOP: Final Product Item Number

SOP: Final Product Item Number

€985.00Price
Excluding VAT

This SOP: Final Product Item Number defines the system for creating and controlling the unique item number assigned to your company’s finished pharmaceutical product. This identifier links all outsourced manufacturing, testing, warehousing, and distribution activities to one consistent product entity, ensuring full traceability, correct documentation, and GMP/GDP compliance.

 

This SOP is professionally written and pre-filled (~95% complete), requiring only company-specific details before approval.

Developed for companies relying on external CMOs, laboratories, and distributors, the template outlines how item numbers are generated, communicated, and maintained — and how changes to formulation, packaging, or configuration trigger reassignment. It also defines responsibilities for QA, Supply Chain, and the Qualified Person (QP).

 

Includes:
• Structure and coding format for product item numbers
• Rules for creation, maintenance, and documentation
• Requirements for communication to CMOs, labs, and logistics partners
• Use of item numbers across batch documentation and labels
• Change control expectations for item number updates

 

Why it matters:
A controlled item numbering system is essential for regulatory compliance, partner alignment, and accurate batch documentation. This SOP ensures your organisation maintains consistent product identification throughout the entire outsourced supply chain.

  • Consulting Support

    If you prefer expert guidance, OZQA provide QA Services, such as:

    • GxP compliance (GMP and GDP)
    • ISO 9001 and ISO 13485 quality systems
    • QMS structure and implementation
    • SOP development and process documentation
    • Deviation, CAPA, Change Control, and OOS processes
    • Audit and inspection preparation
    • Oversight of outsourced partners
  • Product Details & Purchase Terms

    You will receive:

    • Downloadable Word files (.docx)
    • ~98% pre-filled templates
    • Immediate access after purchase

    Important:

    • No refunds (digital product)
    • Requires customization

    Read full Terms and Conditions here.

RELEVANT QUALITY PROCESSES

Need other quality documents?

OZQA provides many regulated documents for pharmaceutical, medical device and other industries that need a compliant QMS. If you can't find the SOP, log form or other quality document on our website - don't hesitate to contact us.

START WHERE YOU ARE

Three ways to build a better QMS.

The OZQA QMS provides ready-to-use quality documents, complete QMS packages designed specifically for regulated companies, and expert quality support. Whether you're starting from scratch, improving an existing system or preparing for your next milestone, we help you focus on what actually matters.

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Ready-to-use quality documents designed for regulated companies. OZQA's editable Word documents are ready for company specific customisation and expandable for later development stages.

DOCUMENTS

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QMS PACKAGES

Start with the full framework

A functioning QMS requires more than SOPs. The package therefore includes relevant supporting documentation to help put the procedures into practice. The documents are designed to work together as one QMS rather than as isolated templates.

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Growing organisations often need Quality expertise long before they need a full internal Quality department. OZQA solutions gives you flexible access to experienced specialists as your needs change.​​​​

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BUILT FOR YOUR NEXT MILESTONE

Wherever you are, we help you move forward.

Quality requirements evolve as products, organisations and regulatory responsibilities develop. What is appropriate before a first clinical trial may no longer be enough at Phase III, just as a MedTech company preparing its first Quality system will have very different needs from one approaching certification or market launch.​​

​OZQA helps you identify what your organisation needs now, while building with the next milestone in mind. Explore the journey for pharmaceuticals to see how Quality systems, documentation, oversight and compliance typically evolve as you move forward.

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