Verification and Validation Requirements for Analytical Laboratory to Comply with ISO IEC Standard 17025:2005
Although method validation and method verification are related terms, they have very different analytical and statistical requirements particularly for compliance with ISO/IEC 17025:2005. Unfortunately, the terms are often incorrectly used interchangeably, resulting in confusion and the application of inappropriate or inadequate analytical evaluations.
The Webinar will discuss the practical distinction between and method validation and method verification and the requirements of each analytical approach to comply with ISO/IEC Standard 17025:2005 for a microbiology laboratory accreditation.
Areas Covered in the Session:
Who Will Benefit:
- The difference between method validation and verification
- The performance characteristics for method validation
- Performance requirements for method verification
- How to implement a verification protocol that defines a method's fitness-for purpose
- Method validation to establish performance characteristics.
- Method Verification to establish analytical competency
- Fitness for purpose
- 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