Analytical Method Validation Under Good Laboratory Practices (GLPs)
This analytical method validation webinar will provide provide practical tips on how to validate an analytical method under the GLP requirements. It is recommended for laboratories that are under, or want to be under, Good Laboratory Practices (GLP). Why Should You Attend: 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. Areas Covered in the Webinar:
Method Validation The criteria for a method Statistical requirements Documentation requirements Common issues
Who will benefit: This webinar will provide valuable assistance to the following personnel from regulated laboratories in pharmaceuticals, chemicals and petrochemicals industry:
Analysts Lab Supervisors and Managers QA managers and personnel Consultants Validation Specialists Chemists
For more information please visit our website: http://www.complianceonline.com/ecommerce/control/trainingFocu s/~product_id=703561/~Analytical_Method_Validation_Under_Good _Laboratory_Practices?channel=DOC http://www.complianceonline.com/