Patient safety is paramount, and CV Labels is certified to PS 9000:2011 – 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.
The key elements of our certificated PS 9000:2011 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.
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.
Production and quality documentation is always available and used to support regulatory compliance.
Our systems help with the integration of any additional regulatory, quality and GMP requirements, ensuring fast, efficient certification.
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.
At CV Labels, we manufacture and supply high-quality labels for a variety of applications across the pharmaceutical, medical and healthcare markets.
The EU Guide to Good Manufacturing Practice (GMP) emphasises the need for pharmaceutical manufacturers and assemblers to ensure the packaging materials they use are of the appropriate quality.
Our ISO 9001:2008 certification ensures we have the essential quality management systems and GMP in place, covering all our key activities.
All jobs are fully traceable to raw materials and pharmaceutical-related production remains segregated, at all times, ensuring product security, integrity and the avoidance of cross-contamination.