DESCRIPTION Analytical instruments should be qualified and systems should be validated to demonstrate suitability for the intended use. This two day in-person seminar will provide attendees the regulatory background and guidance through the complete process from planning and writing requirement specifications to vendor assessment, installation and operational qualification and ongoing testing during routine use. This interactive workshop will help attendees understand the instrument qualification and system validation processes and will provide templates and examples to develop inspection ready documentation. Practical examples and interactive exercises will be dispersed into and between the presentations while 50% of the total time will be dedicated to

Date : 7th December 2017 to 8th November 2017

Place : Gambia The, Amsterdam

Website :https://www.eventbrite.com/e/analytical-instrument-qualification-and-system-validation-com-a-tickets-36929668633?aff=NDT

Contact Person:Paula Edwards

Description:

DESCRIPTION Analytical instruments should be qualified and systems should be validated to demonstrate suitability for the intended use. This two day in-person seminar will provide attendees the regulatory background and guidance through the complete process from planning and writing requirement specifications to vendor assessment, installation and operational qualification and ongoing testing during routine use. This interactive workshop will help attendees understand the instrument qualification and system validation processes and will provide templates and examples to develop inspection ready documentation. Practical examples and interactive exercises will be dispersed into and between the presentations while 50% of the total time will be dedicated to

DESCRIPTION Analytical instruments should be qualified and systems should be validated to demonstrate suitability for the intended use. This two day in-person seminar will provide attendees the regulatory background and guidance through the complete process from planning and writing requirement specifications to vendor assessment, installation and operational qualification and ongoing testing during routine use. This interactive workshop will help attendees understand the instrument qualification and system validation processes and will provide templates and examples to develop inspection ready documentation. Practical examples and interactive exercises will be dispersed into and between the presentations while 50% of the total time will be dedicated to will be held in Amsterdam,Gambia The on date 2017-11-08

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Deadline for abstracts/proposals : 11th December 2017

Keynote Speakers : Dr. Ludwig Huber Chief Advisor - Global FDA Compliance, Labcompliance Dr. Ludwig Huber is Director and Chief Editor of www.labcompliance.com, the global on-line resource for validation and compliance issues for laboratories . Mr. Huber is an expert for FDA and equivalent international compliance and for ISO/IEC 17025 laboratory accreditation. He is also the Chairman, presenter and panel discussion member at US-FDA industry training sessions and conferences. He served as a team member of P

Conference Highlights :Learning Objectives: -Learn about the regulatory background and requirements for laboratory instrument qualification and system validation -Understand the logic and principles of instrument qualification and system validation from validation planning to reporting -Understand and be able to explain your company’s qualification and validation strategies -Be able to independently prepare execute test protocols, this includes setting specifications and acceptance criteria

Venue :Amsterdam, Netherlands

Check the event website for more details.