Seminar on ISO 17025 Document Management Requirements 2016 training seminars presented by Global Compliance Panel register now on FindaSeminar.com

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Seminar on ISO 17025 Document Management Requirements 2016  

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By:

Global Compliance Panel   

For:

Laboratory Management/Supervision, Laboratory Quality Development, Laboratory Quality Management, Laboratory Quality Control, Analytical support

Cost:   

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Seminar Summary:

QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. 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.  (see full course description)

 

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Training Course Syllabus:


ISO 17025 Document Management Requirements 2016

Course "Developing Documents and Records to meet the Requirement of ISO 17025" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant΄s RAC recertification upon full completion.

Overview:

QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. 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.

Why should you attend?

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 needs. 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?


Agenda:

Day 1 Schedule

Lecture 1: Organization Defining a Quality Management System (QMS)
Lecture 2: Management Components of a QMS
• Document Control
• Quality System
• Review of Requests, Tenders and Contracts
• Subcontracting of Tests and Calibrations
• Purchasing Services and Supplies
• Service to Customer
• Control of Non-conforming Testing and/or Calibration Work
• Control of Records
• Internal Audits
• Management Review


Day 2 Schedule:

Lecture 3: Technical Components of a QMS
• Personnel
• Accommodation and Environmental Conditions
• Test and Calibration Methods and Method Validation
• Equipment
• Measurement Traceability
• Sampling
• Handling of Test and Calibration Items
• Assuring the Quality of Test and Calibration Results
• Reporting the Results
• Technical Records

Speaker:

Michael Brodsky
President, Brodsky Consultants

Michael has been an Environmental Microbiologist for more than 43 years. He is a Past President of the Ontario Food Protection Association (OFPA), The International Association for Food Protection (IAFP) and AOAC International.

Seminar Summary:

QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:2005. 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.  (see full course description)

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