Analytical Instrument Qualification and System Validation

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.

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

Who Should Attend

This seminar will be beneficial for the following personnel in pharmaceutical development and quality control laboratories and contract testing laboratories.

Laboratory managers, supervisors and analysts

QA managers and personnel

Quality control unit directors and staff

IT managers and staff

Consultants

Laboratory suppliers of material, equipment and services

Note:

Use coupon code NB5SQH8N and get 10% off on registration.

For Registration:

http://www.complianceonline.com/analytical-instrument-qualification-and-system-validation-seminar-training-80113SEM-prdsm?channel=sciencedz