PS 9000:2016

Patient safety is paramount, and CV Labels is certified to PS 9000:2016 – the application standard developed by the Pharmaceutical Quality Group (PQG) for the manufacture of packaging materials for medicinal products – to ensure they are fit for purpose and safe to use.

The standard is relevant to all parts of the pharmaceutical industry supply chain, and our accreditation is your assurance that the label solutions we deliver will minimise any risk to you and your patients.

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The key elements of our certificated PS 9000:2016 system are:

  • Quality control
    Ensuring a clear implementation of practices across our production process, including electronic interfaces to assure high-quality, fit-for-purpose products.
  • Roles & responsibilities
    Each staff member has a clear understanding of their individual role and responsibilities, in terms of producing quality products.We also make sure that team roles and responsibilities are clearly understood.
  • GMP
    Incorporating Good Manufacturing Practice to ensure materials are of appropriate quality, and that correct procedures are followed in terms of checking, traceability, contamination and hygiene.
  • Risk management
    Our structured approach to the risk management of packaging operations ensures effective controls and mitigation activities are detailed, eliminating or reducing the impact of potential issues.
  • Compliance
    Production and quality documentation is always available and used to support regulatory compliance.
  • Harmonisation
    Our systems help with the integration of any additional regulatory, quality and GMP requirements, ensuring fast, efficient certification.
  • Commitment
    As a company, we are committed to complying with all relevant statutory and regulatory pharmaceutical packaging safety and GMP requirements. This is addition to our own set of rigorous quality standards.