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At BPV Limited, validation is our niche. Our Subject Matter Experts have unparalleled knowledge and experience in providing validation consulting services, setting us apart from other firms such as recruiters recruiting contractors.

Whether you require assistance with validation master plans, validation protocols, or any other aspect of the validation process, our team is ready to help your company achieve its goals while maintaining regulatory compliance.

Our Validation Consulting services extend beyond VMPs and protocol development. We offer project management support, from project initiation to production, validation planning, remediation, and optimisation, as well as deviation management and closure. Our consultants are well-versed in validation methods and processes according to regulatory requirements, ensuring that our clients’ operations are fully compliant.

BPV offers validation consulting services in the UK and to Life Science companies in Ireland. BPV consultants are able to make VMP, validation reports and provide validation protocols.

BPV Limited offers comprehensive Validation Consulting Services to help life sciences companies navigate the complex process of equipment and system validation. Our team of Subject Matter Experts has extensive knowledge and experience in providing Validation Master Plan services, computer systems validation, equipment qualifications, process validation, and test method validation services.

At the core of our Validation Consulting services is the development of robust Validation Master Plans (VMPs) and validation protocols. BPV has its own validation protocols, and clients follow our cGMP-compliant documentation or are able to use their validation protocols. Our consultants work closely with clients to understand their specific requirements and develop tailored VMP that outline the planned validation activities, essential documents, staff responsibilities, and a documented approach for conducting Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) in compliance with cGMP requirements.

The VMPs created by our validation consultants employ risk analysis to establish the scope and extent of qualification protocols, applicable test methods, critical control points requiring evaluation, sampling locations, frequency, and size, as well as schedules for requalification. Key documents included in the VMPs are user requirement specifications, impact assessments, risk analyses, traceability matrices, qualification plans and reports, deviation reports, and final reports.

In addition to Validation Master Plan services, BPV Limited offers assistance with validation throughout the entire lifecycle of equipment and systems. Our full validation package can be customized to suit client needs and typically includes Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Equipment Specific Development Testing, and Requalification packages.

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