Effective Implementation and Internal Audit of ISO/IEC 17025 Laboratory Management System (LMS) and NABL Criteria
Nov 3-6, 2014, Mumbai
Overview
We are delighted to inform you that FICCI Quality Forum (FQF) is conducting training course on Effective Implementation and Internal Audit of ISO/IEC 17025 Laboratory Management System (LMS) and NABL criteria as per the details below:
Date: Nov 03 – 06, 2014
Time: 9.00 am – 6.00 pm.
Venue: Mumbai
This course provides judicious mix of class room presentation, exercises, group discussion, case studies and hand on practice. This course is delivered by best industry experts and recognized by FICCI Quality Forum.
This is a non-residential course of four days duration and concludes with a written examination on the 4th day. Participants successfully completing the continuous assessment during the course and also the written examination will be issued certificate by FICCI Quality Forum.
Eligibility
You should take this course if:
- You want to recognize value of operating effective laboratory management system.
- You are looking to expand your skills in area of laboratory practices.
- You are involved in preparing your organization for assessment /accreditation by NABL.
- You want to conduct LMS audit of your supporting laboratories
Course Fee
Rs. 14,000/- per participant plus 12.36% Service Tax (Total Rs. 15,730/-).
Seats are limited to 20 on first-come-first served basis. Payment can be made through Demand Draft/Cheque in favour of FICCI Quality Forum.
Training Content
1. Introduction
1.1. Certification and Accreditation
1.2. The Global scenario and APLAC, ILAC MRA
1.3. The Process of Laboratory Accreditation.
1.4. Management Requirements of ISO/IEC 17025:2005
1.5. Management Requirements of ISO/IEC 17025:2005
1.6. Detailed examination of important management system elements.
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2. Introduction to Auditing
2.1. Types and methods of Audit
2.2. Checklist preparation, Audit Planning and Audit Schedule.
2.3. The Audit Process |
3. Detailed examination of important technical operations
3.1. Overview of Measurement uncertainty.
3.2. Equipment
3.3. Measurement Traceability.
3.4. Assuring Quality of Test & Calibration results.
3.5. Personnel
3.6. Accommodation and Environment Conditions
3.7. Test & Calibration Methods and method validation.
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4. Identification of Non Conformities
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4.1. Preparation of Audit Report
4.2. The Internal Audit Process
4.3. Implementation of Laboratory Management System with evidence leading to accreditation
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| 5. Technical Requirement of ISO/IEC 17025:2005 Standard |
6. Syndicated exercise on:
a. Management Requirement
b. Developing Documented Procedure
c. Technical requirements
d. Developing standard operating procedure
e. Internal Audit
f. Identification and writing of Non-conformities
g. Corrective action close out of non conformities
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