LIMS Validation is a buzzword that tends to be widely misunderstood, and much abused, in the laboratory industry. And yet it is an important and challenging task. The US Food and Drug Administration (FDA), equivalent worldwide regulatory bodies and many certification bodies such as ISO, require that software systems be tested and proven to work as intended. LIMS validation is therefore a vital step in regulated environments, certified laboratories, and best practice laboratories to ensure data integrity and prove compliance. In this webinar we will debunk the myths and explain how you can drive validation of your LIMS system.
• What is LIMS Validation?
• When is LIMS Validation needed?
• A typical LIMS Validation process
• Consulting vs in-house resources
• Configuration GAMP categories, what you need to know
• Planning your LIMS Validation
This webinar is for all who use LIMS for any kind of quality assurance. You will discover a methodology to drive a risk-based approach to LIMS validation and be armed with the information you need to take the next steps confidently.
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