FDA Regulations for Analytical Instrument Qualification and Validation Processes 2017
17 Oct 2017
Webinar
Description
Topics
Risk based validation approach
Requirements and approaches for Analytical Instrument Qualification
User requirements, writing the specifications
Going through the qualification phases
Proper documentation
Testing and deviation handling
Periodic review and revalidation analytical instruments and equipment
Type and extend of qualification for USP Instrument Categories
Wrap up - Final questions and answers
Who should Attend
IT managers and staff
Laboratory managers, supervisors and analysts
Laboratory suppliers of material, equipment and services
Consultants
Quality professionals
Senior quality managers
Compliance professionals
Regulatory professionals
Validation engineers
Production supervisors
Production engineers
Manufacturing engineers
Process owners
Design engineers
Quality auditors
Quality engineers
Past Events
FDA Regulations for Analytical Instrument Qualification and Validation Processes 2017 - 17 Oct 2017, Webinar (66589)
Important
Please, check "FDA Regulations for Analytical Instrument Qualification and Validation Processes" official website for possible changes, before making any traveling arrangements
