Why and How - Verification of Compendial Methods
This webinar will provide an in-depth discussion of USP <1226>, 'Verification of Compendial Methods' requirements. We will discuss FDA 483s on the subject of Method Verification to understand current FDA expectations. Why Should You Attend: This webinar will provide an in-depth discussion of USP <1226>, 'Verification of Compendial Methods' requirements. Conditions under which Methods can be classified as 'basic' and not require verification will be discussed. The factors under actual conditions of use which impact method performance and make method verification necessary will be addressed. FDA 483s on the subject of Method Verification will be discussed to understand current FDA expectations for verification of compendial methods. Areas Covered in the Webinar:
FDA 483s related to method verification. Requirements of USP <1226>, 'Verification of Compendial Methods' What are the current FDA expectations related to method verification. What are the factors which impact method performance under actual condition of use?
Who Will Benefit:
QC personnel QC Supervisors and Management QA personnel QA Management Documentation management specialists Regulatory affairs personnel R&D Lab personnel R&D Lab Supervisors
For more information please visit our website: http://www.complianceonline.com/ecommerce/control/trainingFocu s/~product_id=701752?channel=DOC