Analytical Instrument Qualification and System Validation: 2- day In-person Seminar

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.

• 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

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

Use coupon code 232082 and get 10% off on registration.