CQV Pharmaceutical, Life Science and Biotechnology Services
Established over 21 years ago, Bailey Services has wide and varied experience in commissioning, qualification and validation services to the UK’s pharmaceutical, biotechnology and life science industries. Our CQV engineering teams provide a flexible and thorough service to leading pharmaceutical and medical clients, and small specialist companies, ensuring compliance with government standards, and guaranteeing public safety.
CQV Pharmaceutical & Biotechnology Services
With an extensive network of the best CQV engineering professionals in the UK biotechnological services and life sciences industry, we can quickly get up to speed on your ways of working and integrate seamlessly into your operation. As part of our comprehensive CQV pharmaceutical consulting services, we leverage our large network of Subject Matter Experts and Project Managers to provide clients with comprehensive end-to-end project, assessment, and decommissioning solutions.
We actively promote lean, science and risk-based life cycle approaches to our biotechnological services, including ASTM E2500, GAMP 5 and QbD methodology. Our emphasis is on providing you with the right commissioning, qualification and validation solutions to achieve your objectives. We understand the need to be proactive in response to change during life science pharmaceutical and biotechnology projects, assess risk, identify options and deliver projects on time, within budget, whilst maintaining quality and safety at all times. Everything we do is to help you stay compliant with all UK legislation.
We actively promote lean, science and risk-based life cycle approaches
including ASTM E2500, GAMP 5 and QbD methodology.
About BSL
Bailey Services (BSL) was incorporated in April 2001, a team of CQV engineers operating primarily within the UK CQV Life Science pharmaceutical industry with experience in the commissioning and qualification of Pharmaceutical, Biotechnology services and Chemical Plants including facilities, utilities, laboratories and associated control systems.
Our experienced CQV engineers have an excellent track record of providing a range of services to organisations of all sizes across the country. All our CQV and biotechnology consulting contracts are completed in compliance with the IR35 Off Payroll Legislation and other government codes of conduct. Our areas of specialism include medical devices, active pharmaceutical ingredients (APIs), advanced therapy medicinal products (ATMPs) and the validation of chemical plants.
Documentation
Accuracy and consistent quality are prioritised in every CQV documentation package we provide. This service is adaptable to the needs of your individual project, and includes drafting of policies and protocols, ensuring that processes run efficiently and comply with applicable regulations, current regulatory guidance and GMP/GEP.
Decommissioning
During every decommissioning process in the life sciences pharmaceuticals and biotechnology industry, we consider compliance, finance, maintenance and communications with stakeholders.
Our CQV engineers manage the process of retiring equipment and facilities in a way that is safe, cost-effective and compliant to Good Manufacturing Practices (GMP) and Good Engineering Practices (GEP).
Reviews
When CQV periodic reviews are required for pharmaceutical equipment and processes including those that carry a high risk, we work thoroughly and in accordance with applicable regulations and guidelines.
Risk Assessments
Our biotechnology consulting services include quality risk management processes, in order to identify areas of risk to product quality and patient safety in equipment, facilities, processes and systems.
Contact Us
For further information about our CQV pharmaceutical and biotechnology consulting services, please complete the contact form here.