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Analytical Method Validation Under Good Laboratory Practices – GLPS

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Contact Person – Compliance4all

Event inquiry /Organizer email address – compliance4all14@gmail.com

Organized by: Compliance4all

Topic Covered: Medicine and Medical Science

Event Start Date – 03rd Aug 2021

Deadline for abstracts/proposals: 03rd Aug 2021

Event End Date – 03rd Aug 2021

Venue: Fremont, United States of America

About Event:

Overview: If you do any work that will be reported to the US Food and Drug Administration FDA, Environmental Protection Agency EPA, or Occupational Safety and Health Administration OSHA, your work must be done under GLP. All methods must be validated, the proof that they do what is claimed. Common criteria are accuracy, precision, linearity, range, and several more. This webinar will discuss the best practices of analytical method validation, including components of a validation, how to include critical reagents comparison, selectivity experiments, assessment of stability, importance of communication between the development and the validation labs and accuracy of transfer documents SOPs. Participants will understand – Is validation a regulated activity? When to pull the trigger for validation? Importance of suitability testing.



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