Calibration and Qualification in Analytical Laboratories
July 8, 2015 - Online event CA USCompliance4all
support@compliance4All.com
Phone:8004479407
Fax:302-288-6884
Overview: Laboratory equipment should be calibrated and/or qualified to demonstrate suitability for the intended use. Laboratory systems including equipment are amongst key targets of FDA inspections. They are considered high risk systems because they have a high impact on product quality. Despite the fact that equipment calibration and qualification is nothing new and companies spend a lot of time, it is a frequently cited deviation in FDA inspectional observations and warning letters. Companies are unsure on what exactly to qualify, test and document. For easy implementation, attendees will receive: 4 SOPs User Requirement Specifications (URS) for analytical equipment Change control for analytical equipment Qualification of equipment Allocating Analytical Instruments to USP <1058> Categories 20+ Examples for Instrument OQ Testing Read more : http://www.compliance4all.com/control/w_product/~product_id=500398LIVE/