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Validation of Analytical Methods and Procedures - Webinar

  • ID: 4061791
  • Webinar
  • June 2018
  • Region: Global
  • 75 Minutes
  • NetZealous LLC
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Analytical methods should be validated to ensure reliability, consistency and accuracy of analytical data. Method validation has been a requirement of FDA and international regulations and accreditation standards such as ISO 17025 since many years and new official guidelines have been published by FDA, EMA and USP in the last 4 years. Most often the theory is well understood but there are many questions when validation experiments are designed, conducted, and documented.

This webinar will provide a good understanding on how to effectively conduct and document method validation, method re-validation and periodic review.

Reference Material for Easy Implementation

SOP: Transfer of Analytical Methods
Checklist: Transfer of Analytical Methods and Procedures
Master Plan Template and Examples: Transfer of Analytical Methods and Procedures

Areas Covered in the Session:
Current and new guidelines from FDA, WHO, EMA and USP
Examples of warning letters and how to avoid them
Developing an SOP for method validation
Development of a validation plan for success
Prerequisites for method validation
Defining the minimum number of validation experiments that satisfy ICH, FDA and USP
Defining test conditions and acceptance limits
Verification of compendial methods according to USP < 1226>
To revalidate or not after method changes
Ensuring on-going method performance through periodic review
Transferring a method to routine according to USP < 1224>
Seven most common method validation pitfalls and how to avoid them
Documentation for the FDA and for other agencies
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  • Laboratory Managers and Supervisors
  • GLP/GCP/GMP Auditors
  • ISO 17025 Auditors
  • QA/QC Managers and Personnel
  • Analysts and Other Laboratory Staff
  • Regulatory Affairs
  • Training Departments
  • Consultants
Note: Product cover images may vary from those shown