Validation refers to establishing documented evidence that a process or system, when operated within established parameters, can perform effectively and reproducibly to produce a medicinal product meeting its predetermined specifications and quality attributes
Tuesday, January 2, 2018
Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements
Click here for more Information http://ift.tt/2CD8O7X Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements Presented By: Roger Cowan The session will review different filtration media and will discuss in detail the construction characteristics and properties of each. You will get a detailed description of a typical pharmaceutical sterile filtration system with its individual components, including a discussion on engineering schematics. More Videos: - http://www.youtube.com/user/audioeducator2 You can also connect with us on Twitter, Facebook, Google+ and LinkedIn and get the most updated news and views, expert advice and tips to help resolve your coding, billing & compliance dilemmas quickly and accurately. Connect with us on Twitter: - https://twitter.com/audioeducator Facebook: - http://ift.tt/2lzPCk2 LinkedIn: - http://ift.tt/2qaJ2oX Google+: - http://ift.tt/2lzPGAi
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