This webinar will discuss the distinction between and requirements for method validation and method verification, to comply with ISO/IEC Standard 17025:2005 for laboratory accreditation in food/water microbiology.
Method validation and method verification are two distinct procedures required to combat food bioterrorism/ comply with ISO/IEC Standard 17025:2005 for a microbiological media laboratory accreditation and microbiological contamination control in pharmaceutical clean rooms.
Unfortunately, the two terms are often used interchangeably with serious consequences in bioterrorism food and FDA inspection readiness checklist.
Without a clear understanding of the different analytical approaches for verification and validation, laboratories often end up doing more unnecessary, costly work, with little benefit for FDACGMP compliance, FDA audit training, FDAGMP compliance or for FDA good documentation practices.
Very often the inappropriate analytical strategy used is unacceptable to meet the requirements for FDA validation training/ accreditation and the effort needs to be repeated. Learn to do the microbiology media preparation, right the 1st time!
For more info and registration visit www.atozcompliance.com