tag:blogger.com,1999:blog-6889368780602598071.post4592966932997160651..comments2024-03-14T16:57:22.287+05:30Comments on Quality Assurance, GMP and Pharma Jobs: Cleaning Validation ProcedureQuality Assurance and GMPhttp://www.blogger.com/profile/13093846178697640897noreply@blogger.comBlogger1125tag:blogger.com,1999:blog-6889368780602598071.post-27143088451391809242014-12-01T16:07:24.246+05:302014-12-01T16:07:24.246+05:30Any single group must be subjected to the 3 valida...Any single group must be subjected to the 3 validation cleaning requirement,<br />except if a rationale is recorded and also approved by the Standard Authority <br />which the worst-case product of one group is clearly a worst-case product for every one of the groups.<br />Software validation is a part of the design validation for a finished device,<br />but is not separately defined in the Quality System regulation.<br /><br /><br /><a href="http://automationandvalidation.com" rel="nofollow">equipment validation</a><br /><a href="http://automationandvalidation.com" rel="nofollow">labview programming</a><br /><a href="http://automationandvalidation.com" rel="nofollow">software validation</a><br />jackbroobgmhttps://www.blogger.com/profile/14871222478895818560noreply@blogger.com