3-hr Virtual Seminar: Developing Documents and Records to Meet the Requirements of ISO,IEC 17025
Duration : 3 Hours
Michael Brodsky,
Michael has a post-graduate degree from the University of Toronto, School of Hygiene and Tropical Medicine and been an Environmental Microbiologist for more than 46 years, as a research scientist and Laboratory Director in both the public and private sector. He currently operates as the President Read more
QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. Accreditation to international standards is being becoming the norm in the global analytical community. Although essentially voluntary, there are many jurisdictions that now require food and environmental laboratories to be accredited to ISO/IEC 17025 in order to participate in regulatory programs. Many laboratories struggle with developing and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their own needs and those of their customers. Once accreditation has been achieved many laboratories have difficulty maintaining the QMS as evidenced by the number of non-conformances cited during the subsequent biannual audits. Why do you want to become accredited? Where do you start? For laboratories that are already accredited, how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits? The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the “what to do” component of a QMS. What is also needed are the “how to do it” or procedures and methods and finally the controls or evidence that it was done properly.
Course Objectives:
• Policies
o KISS principle
• Procedures
o The devil’s in the details
• Records
o The proof is in the pudding
Course Outline:
• How to Document the Management Components of a QMS
o Document Control
o Quality System
o Review of Requests, Tenders and Contracts
o Subcontracting of Tests and Calibrations
o Purchasing Services and Supplies
o Service to Customer
o Control of Non-conforming Testing and/or Calibration Work
o Control of Records
o Internal Audits
o Management Review
• Records Needed to Meet the Technical Components of a QMS
o Personnel
o Accommodation and Environmental Conditions
o Test and Calibration Methods and Method Validation
o Equipment
o Measurement Traceability
o Sampling
o Handling of Test and Calibration Items
o Assuring the Quality of Test and Calibration Results
o Reporting the Results
o Technical Records
What You Get:
• Training Materials
• Live Q&A Session with our Expert
• Participation Certificate
• Access to Signup Community (Optional)
• Reward Points
Who Will Benefit:
• Laboratory Management/Supervision
• Laboratory Quality Development
• Laboratory Quality Management
• Laboratory Quality Control
• Analytical support
Please reach us at 1-888-844-8963 for any further assistance or if you wish to register
