Bio Products Validation Ltd (BPV) was established with the focus of offering the best level of validation services within the UK and Ireland Life Science industry. With a dedicated team of validation engineers and consultants, the BPV limited team has provided services to the life science industry since 2005.
BPV limited specialises in Sterilisation Validation Services, Equipment Validation Services, Computer System Validation Services (CSV services), Processes Validation Services, Cleaning Validation Services, and Thermal Mapping.
Commissioning, Qualification and Validation (CQV) Services
We validate a wide range of equipment and processes, including Autoclaves, Lyophilisers, Depyrogenation Tunnels, Clean/ Steam in place, CSV and Serialisation. We cover the whole equipment lifecycle including Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) and development testing.
We work closely with you whether that be through...
• Working with our in-house validation engineers and consultants • Hire of pre-approved validation contractors • Validation equipment hire • Validation consultancy
BPV’s Commitment To Quality
Quality is a core value at our company. We strive to improve the validation services industry-wide through comprehensive testing, reporting, and active participation in enhancing validation standards.
Our employees and contractors stay updated on cGMP requirements, and we undergo regular audits for ISO9001 certification and client audits to maintain high-quality levels.
Benefits of Working with BPV Limited
• Time savings: outsourcing your validation work to us will save time compared to internally sourcing engineers for validation services. We have a pool of exceptional validation engineers who you can rely on, saving you time in the long run.
• Cost Savings: Improved reliability, equipment efficiency and reduced downtime due to quality development testing can lead to cost savings.
• Fully independent validation service: removing the risk of bias that can occur when using stakeholders with a vested interest in equipment passing the qualification.
• Fully compliant with cGMP and GxP requirements: As partners to the industry, we ensure that all of our employees have an up-to-date understanding of cGMP and GxP requirements, ensuring high levels of compliance.
• Flexibility and scalability: We have a pool of 400+ validation engineers and the ability and expertise to scale up /down your projects quickly as needed. This can be especially advantageous when facing fluctuating workloads or short-term projects.
• Deep expertise specific to the Pharmaceutical and Life Science industry: We endeavour to meet your specific requirements, often placing the person with the most expertise in working with a particular piece of equipment on your project to ensure you get the best possible service.
• Commitment to Quality: We achieve and maintain quality standards by providing ongoing training for all employees and contractors. We are also ISO 9001 certified and fully auditable.
• Trusted by the industry: We have partnered with many well-known enterprises in the industry, but still ensure we provide a customised solution for every client.
