tag:blogger.com,1999:blog-233439135322711757.post6815388711380396266..comments2024-03-28T04:43:04.966-07:00Comments on Pharmaceutical Validation: The Validation and Implementation of a Chromatography Data System 1Princehttp://www.blogger.com/profile/18347371720617709214noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-233439135322711757.post-15293830768762626112013-03-09T10:45:46.589-08:002013-03-09T10:45:46.589-08:00Bio-Med and Pharmaceutical Validation can be very ...Bio-Med and Pharmaceutical Validation can be very simple and straight forward, and then again at times, it can be complex and difficult. A great deal depends on the contents of the company Corporate Quality Manual. This is where all company approved bio-med and pharmaceutical validation regulatory Practices and Procedures must be defined and documented. Failing this being in place, the VMP and Bikramhttps://www.blogger.com/profile/03007323568196311495noreply@blogger.comtag:blogger.com,1999:blog-233439135322711757.post-40074685658049041522013-01-14T05:58:36.758-08:002013-01-14T05:58:36.758-08:00This process involves the assessment of the applic...This process involves the assessment of the application against the user requirements. This may include a vendor audit, which encompasses IT and regulatory requirements. With the advent of 21 CFR Part 11, this became a prerequisite before a final decision could be made. <a href="http://www.automateandvalidate.com" rel="nofollow">more information</a>Anonymoushttps://www.blogger.com/profile/06113020028758761548noreply@blogger.com