CQV制药,生命科学和生物技术服务
成立于21年前, 贝利服务公司在调试方面拥有广泛而多样的经验, 为英国制药公司提供鉴定和验证服务, 生物技术和生命科学产业. Our CQV engineering teams provide a flexible and thorough service to leading pharmaceutical and medical clients, 小型专业公司, 确保符合政府标准, 保障公共安全.
CQV制药 & 生物技术服务
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. 作为澳门维加斯手机网址综合CQV医药咨询服务的一部分, we leverage our large network of Subject Matter Experts and Project Managers to provide clients with comprehensive end-to-end project, 评估, 退役解决方案.
澳门维加斯手机网址积极提倡精益, science and risk-based life cycle approaches to our biotechnological services, 包括ASTM E2500, GAMP 5和QbD方法. 澳门维加斯手机网址的重点是为您提供正确的调试, 确认和验证解决方案,以实现您的目标. We understand the need to be proactive in response to change during life science pharmaceutical and biotechnology projects, 评估风险, 确定选项并按时交付项目, 在预算之内, 同时始终保持质量和安全. Everything we do is to help you stay compliant with all UK legislation.
澳门维加斯手机网址积极提倡精益, science and risk-based life cycle approaches
包括ASTM E2500, GAMP 5和QbD方法.
对澳门维加斯手机网址
贝利服务(BSL)成立于2001年4月, a team of CQV engineers operating primarily within the UK CQV Life Science pharmaceutical industry with experience in the commissioning and qualification of Pharmaceutical, 生物技术服务和化学工厂包括设施, 公用事业公司, 实验室和相关的控制系统.
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. 澳门维加斯手机网址的专业领域包括医疗器械, 活性药物成分(api), advanced therapy medicinal products (ATMPs) and the validation of chemical plants.
文档
Accuracy and consistent quality are prioritised in every CQV documentation package we provide. 此服务可适应您的个人项目的需要, 包括起草政策和协议, ensuring that processes run efficiently and comply with applicable regulations, 现行法规指导和GMP/GEP.
退役
During every decommissioning process in the life sciences pharmaceuticals and biotechnology industry, 澳门维加斯手机网址考虑遵守, 金融, 维护和与利益相关者的沟通.
Our CQV engineers manage the process of retiring equipment and 设施 in a way that is safe, cost-effective and compliant to Good Manufacturing Practices (GMP) and Good Engineering Practices (GEP).
评论
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.
风险评估
Our biotechnology consulting services include quality risk management processes, in order to identify areas of risk to product quality and patient safety in equipment, 设施, 流程和系统.
澳门维加斯手机网址
For further information about our CQV pharmaceutical and biotechnology consulting services, 请填写联络表格 在这里.