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Auditing Analytical Laboratories for FDA Compliance 2017
20-21 Nov 2017
Manila, Philippines
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Auditing Analytical Laboratories for FDA Compliance 2017
Description
Topics
Reviewing Documentation
GMP Regulations that Apply to Analytical Laboratories
Auditing Styles and Structures
Advance Preparation for the Audit
What to look for while doing a Walk-Through
Equipment and Laboratory Instrument Qualification
Following through on the Audit
Other Regulations and Standards, including ISO 17025
Who should Attend
Supervisors and Analysts in Quality Control Laboratories and Quality Assurance groups
External and Internal Auditors
Personnel Responsible for Selecting Contract Testing Laboratories
Supervisors and Analysts in Contract Testing Laboratories
Consultants
Past Events
Auditing Analytical Laboratories for FDA Compliance 2017 - 20-21 Nov 2017, Manila, Philippines
(70937)
Important
Please, check "Auditing Analytical Laboratories for FDA Compliance" official website for possible changes, before making any traveling arrangements
Event Categories
Business:
Internal Audit & Compliance, Quality assurance
Health & Medicine:
Medical laboratories
Science:
Laboratories
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