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Main Equipment Validation, Tracking, Calibration, and Preventive Maintenance
Equipment Validation, Tracking, Calibration, and Preventive Maintenance Instructor : Jeff Kasoff
Product Id : 600570
Duration: 60 Minutes
Wednesday, December 14, 2011 Overview: FDA and EU regulations require that firms have a program for the calibration and maintenance of test and measurement equipment. The program must include: intervals, scheduling, specific procedures, limits of accuracy/precision, and remedial action in the event that the equipment does not meet established requirements. Prior to use, however, this equipment must be validated to make sure it produces product that meets its specifications. However, there are ways to validate equipment already in use!
10:00 AM PST | 01:00 PM EST
b Live live online training only for one participant c d e f g Price: $245.00
c Corporate Live 6 to 10 participants from a single d e f g
location (For multiple locations contact Customer Pack of THREE: Best Selling Webinars by GlobalCompliancePanel
Care) Price: $995.00
Price: $495.00 Areas Covered in the Session: Equipment Validation: Installation Qualification, Operation Qualification, and Performance Qualification
g Recorded Access recorded version only for one c d e f participant; unlimited viewing for 6 months ( Access
Equipment Calibration Requirements
information will be emailed 24 hours after the
Equipment Preventive Maintenance Requirements
completion of live webinar)
Calibration vs. Maintenance: When to use Which One?
Pack of THREE: Best Selling DHFDMR-DHR Webinars by GlobalCompliancePanel Price: $495.00
Remedial Action for Out-of-Calibration Equipment Use of Calibration Standards to Save Cost Refund Policy Who Will Benefit: This webinar will provide valuable assistance to all personnel involved in process development: R&D management Engineering management Production management Production engineers R&D engineers
Customer Testimonials Some of these sessions are too basic - this one had a good mix of basic and details. The tips are helpful. One comment: a little more discussion regarding the use of Detection in FMEAs would be useful since many do not advocate its use. Thanks,
Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy products. In this position, Jeff is responsible for supplier management, during which he reviews and approves supplier qualification, selection, assessment, and CAPA. Prior to this, Jeff spent 13 years at Life-Tech as the Director of Regulatory Affairs, where he was responsible for regulatory compliance of all aspects of the quality system. Jeff received his regulatory affairs certification in 1996.
I especially liked that the Q&A session after the webinar was long enough to not only
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Published on Nov 15, 2011
The program must include: intervals, scheduling, specific procedures, limits of accuracy/precision, and remedial action in the event that th...