Share Your Research, Maximize Your Social Impacts
Main Menu
Searching By
PARTNERS
Online Training 2015 - Is it Method Verification or Validation, or Just Semantics? - By Compliance Global Inc
Date2015-06-30
Deadline2015-06-30
VenueCompliance Global Inc. 2754 80th Avenue, New Hyde Park, NY 11040, USA - United States 
KeywordsVerification methods; Lab accreditation; Environmental laboratory
Topics/Call fo Papers
Overview:
The Webinar will discuss the distinction between and requirements for method validation and verification methods, to comply with ISO/IEC Standard 17025:2005 for a microbiology laboratory.
Why Should You Attend:
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.
Areas Covered in the Session:
? Method validation to establish performance characteristics.
? Method Verification to establish analytical competency
? Fitness for purpose warranty
Learning Objectives:
Upon completion of this session, attendees will learn
? 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
Who Will Benefit:
? Quality Assurance Managers
? RA & AC Professionals
? Laboratory Managers
? Laboratory Supervisors
? Personnel responsible for Developing/Implementing Microbiological Methods
Level:
Intermediate
For more detail please click on this below link:
https://www.complianceglobal.us/product/700131
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
The Webinar will discuss the distinction between and requirements for method validation and verification methods, to comply with ISO/IEC Standard 17025:2005 for a microbiology laboratory.
Why Should You Attend:
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.
Areas Covered in the Session:
? Method validation to establish performance characteristics.
? Method Verification to establish analytical competency
? Fitness for purpose warranty
Learning Objectives:
Upon completion of this session, attendees will learn
? 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
Who Will Benefit:
? Quality Assurance Managers
? RA & AC Professionals
? Laboratory Managers
? Laboratory Supervisors
? Personnel responsible for Developing/Implementing Microbiological Methods
Level:
Intermediate
For more detail please click on this below link:
https://www.complianceglobal.us/product/700131
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Other CFPs
- Proof It! How To Be a Better Proof reader. - By Compliance Global Inc
- How to Conduct a Proper HIPAA Security Risk Assessment and Write Policies Based on the Findings. - By Compliance Global Inc
- Employee’s Nationalization (Resident and Non Resident) Status for Purposes of Payroll. - By Compliance Global Inc
- Review of Employee Grievance Laws and Techniques for Avoiding Complaints. - By Compliance Global Inc
- FSMA Rules in Dairy Logistics - Food Safety in Storage and Transportation. - By Compliance Global Inc
Last modified: 2015-06-05 14:03:06