as in the title you t as inflation rises as intimate as ones o as is well known as o as it progresses as it swallowed all i as it travels as its core philosoph as its idea as ivy po ling as jimmy said as legend would have as lieutenant colonel as long as i gaze on as long ...
Agilent is a global leader in life sciences, diagnostics and applied markets, recognized for uncompromising integrity in all we do. Our mission is to advance quality of life by focusing our expertise in six key markets. With a team of approximately 18,000 employees spread across the world, our...
It is the policy of WHO not to assign an expiry date to their international reference materials. They remain valid with the assigned potency and status until withdrawn or amended.Reference materials are held at NIBSC within assured, temperature-controlled storage facilities. Reference Materials should ...
8.4. Because the toxicity of some materials may not be fully known, cleaning is of particular importance. Validated cleaning procedures should be followed in order to prevent cross- contamination. The visual inspection after cleaning, sampling and test procedures should be appropriate and the acceptanc...
Top/senior management has the responsibility of ensuring an effective QMS is in place, is adequately resourced, and that roles, responsibilities, and authorities are defined, communicated and implemented throughout the organization. 高层/高级管理人员有责任确保有效的质量管理体系,配备有充足的资源,并确保角...
This is applicable to legacy products as well as the introduction of new products introduced into a facility through a change control procedure. 这适用于在产产品以及通过变更控制程序引入的新产品。 Procedures should be established and implemented describing how scientific data and toxicological information...
3.8. The main focus of the document is on pharmaceutical formulation and development. The principles described in this document may however be applied in facilities where other products such as vaccines, veterinary products and biopharmaceutical products are developed. The principles may also be consider...
近日,WHO发布了新的清洁验证指南——《不同方法——包括HBEL——建立清洁验证的残留限度以确定共用设施生产污染风险的考量》,该指南解读如下:收集样品的地点(擦拭取样)及方式应清楚说明,并具科学理据支持。 …
1.2 The focus of this document is on the treatment, storage and distribution of treated water used in pharmaceutical applications. It excludes the production, storage and usage of water in qualit y-control laboratories. 本文重点 在于制药用水 的生产、储存和分配 ,不包括质量控制实验室 用水 的生产...
transfer 阶段3 项目转移 • Production: transfer (processing, packaging) • 生产:转移(工艺、包装) • Starting materials • 起始物料 • Active pharmaceutical ingredients • 活性药物成分 • Excipients • 辅料 • Information on process and finished pharmaceutical products information • 关于...