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17025Pro Accelerator Pack: Comprehensive Course with Custom Documents
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What Will You Learn?
- Basics of ISO/IEC 17025: Understand the core principles, requirements, and applications for laboratory compliance.
- Uncertainty Measurement: Master methods for calculating and managing measurement uncertainty in your lab.
- Calibration Process: Learn best practices for calibration, including standards, equipment, and procedures.
- Internal Audits: Gain the skills to conduct effective internal audits, including preparation, execution, and reporting.
- 100+ ready-to-use documents: including SOPs, clause-wise forms, and an uncertainty calculator, to streamline ISO 17025 compliance.
Course Content
Introduction to ISO 17025:2017
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Download Document Tool-Kit
-
ISO 17025 Background
01:20 -
What is ISO 17025?
00:48 -
Terms
01:45 -
Interlaboratory comparison
01:04 -
Decision Rule
01:45 -
Validation
00:34 -
General Requirements
01:16 -
Structural Requirements
01:26 -
Resource Requirements
02:11 -
Resource Requirements Part-2
01:40 -
Process Requirement
01:37 -
Sampling
01:24 -
Measurement Uncertainty
02:14 -
Complaints
01:12 -
Management System
00:55 -
Management Requirement
00:57 -
Management Requirement part-2
00:57
Uncertainty Measurement
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What is Uncertainty?
01:51 -
Error vs Uncertainty
01:06 -
Normal Distribution
00:53 -
Measurement Traceability
00:55 -
Sources of Uncertainty
00:55 -
How to reduce Uncertainty?
00:45 -
Standard Deviation
01:25 -
Precision vs Accuracy
01:17 -
Combined Uncertainty
01:53 -
Confidence level
04:21 -
Uncertainty Influence Factors
02:34 -
Reporting Uncertainty
02:58 -
Types of Distribution
02:43 -
Uncertainty Budget
01:44 -
Uncertainty terminology
03:17 -
Measurement Process
02:15 -
Uncertainty Component (SWIPE method)
01:54 -
Type A Uncertainty
01:26 -
Standard Uncertainty
02:01 -
Distribution
02:16 -
Degree of freedom
01:44 -
K Value
01:45 -
Expanded Uncertainty
01:29
Calibration Process
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What is Calibration?
03:18 -
Purpose of Calibration
02:46 -
Calibration Planning
03:56 -
Calibration Standard
02:28 -
Calibration Procedure
02:54 -
Common Measuring Instrument
05:54 -
Traceability
03:36 -
Preparation
03:06 -
Calibration Certificate
03:22 -
Importance of Calibration
03:07 -
Calibration labels
03:01 -
New Techs
04:44 -
Physical System
02:47 -
Benefits
05:10 -
Calibration Personnel
02:35 -
Common Lab Practice
02:12 -
Lab Environment
02:57
Internal Audit
-
Terms in Internal Audit
03:07 -
Objective of Internal Audit
01:46 -
How to Organize ?
02:14 -
Audit Planning
01:52 -
Why Do Internal Audit?
02:46 -
Implementation of Internal Audit
02:22 -
Corrective Actions
01:51 -
Audit Reports
01:59 -
Non-Conformity Management
02:52
E-Books(Downloads)
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Clause vs Document Checklist
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Minimum Checklist for Internal Auditor
Quality Manual (Download)
-
Quality Manual
SOPs (Downloads)
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Calibration Methods
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Corrective Action
-
Customer Service
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Document Control
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Evaluating Measurement Uncertainty
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Handling Complaints
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Handling Equipment
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Improvement Monitoring
-
Internal Audit Procedure
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Internal Quality Checks
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Lab Equipment Handling
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Maintaining Accommodation and Environmental Conditions
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Maintaining Customer Confidentiality
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Maintaining Impartiality
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Management Review
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Managing Personnel
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Non-Conformance Work
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Purchasing Management
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Quality Assurance (QA) Procedure
-
Records Control
-
Result Reporting
-
Reviewing Contracts
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Managing Risk and Opportunity
Clause wise Forms (Downloads)
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Intermediate Check of Instruments (Clause 6.4)
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Calibration Schedule Record for Monitoring and Measuring Instruments (Clause 5.6)
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Job Matrix (Clause 6.2)
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Personnel Vitae (Clause 6.2)
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Training Attendance Sheet (Clause 6.2)
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Training Calendar (Clause 6.2)
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List of Authorized Personnel for Testing (Clause 6.2)
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Effective Evaluation of Personnel (Clause 6.2)
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Training Feedback (Clause 6.2)
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Daily Cleaning Record (Clause 6.3)
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Breakdown Maintenance Record (Clause 6.4)
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Equipment History Card (Clause 6.4)
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Frequency of Intermediate Checks (Clause 6.4)
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Intermediate Check List Record (Clause 6.4)
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Maintenance Schedule Record (Clause 6.4)
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Preventive Maintenance Record (Clause 6.4)
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List of Reference Standards (Clause 6.5)
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Approved Supplier List (Clause 6.6)
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Incoming Inspection Record (Clause 6.6)
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Supplier Evaluation Record (Clause 6.6)
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List of Approved Subcontractors (Clause 6.6)
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Purchase Requisition (Clause 6.6)
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Supplier Registration Format (Clause 6.6)
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Sample Testing Request (Clause 7.1)
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Sample Library Register for Testing (Clause 7.3)
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Master List Retention of Record (Clause 7.6)
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Replicate Test (Clause 7.7)
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ILC (Inter-Laboratory Comparison) Summary Sheet (Clause 7.7)
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Replicate Testing (Clause 7.7)
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Retesting (Clause 7.7)
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Schedule Planning for Inter-Laboratory Comparison (ILC) (Clause 7.7)
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Inter-Laboratory Test (Clause 7.7)
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Retesting of Retained Sample (Clause 7.7)
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Customer Complaint Form (Clause 7.9)
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Customer Feedback Form (Clause 7.9)
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Customer Feedback Analysis (Clause 7.9)
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Improvement Trends Analysis (Clause 7.10)
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Non-Conforming Testing Work Record (Clause 7.10)
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Non-Conformity Report (Clause 7.10)
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Near Miss Report (Clause 7.11)
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Document Change Request Form (Clause 8.3)
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Master List of Documents (Clause 8.3)
-
Objective Monitoring (Clause 8.3)
-
Quality Objective Monitoring Status (Clause 8.3)
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Corrective Action Report (Clause 8.7)
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Internal Audit Schedule (Clause 8.8)
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Audit Summary Report (Clause 8.8)
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Internal Audit Plan (Clause 8.8)
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Internal Auditor List (Clause 8.8)
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Retesting Witnessed by Internal Auditor During Internal Audit (Clause 8.8)
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Management Review Meeting (MRM) Plan (Clause 8.9)
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Appointment Letter of Quality Manager
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First Aid Box (Clause 6.3)
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Request Letter for Approved Subcontractor for Testing (Clause 6.4)
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Supplier Evaluation and Monitoring (Clause 6.6)
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Raw Data Register (Clause 7.4)
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Risk Analysis Register (Clause 8.5)
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Opportunity Identification and Review Register (Clause 8.5)
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Internal Audit and MRM Plan (Clause 8.8)
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Review of Annual General Contract for Testing (Clause 7.1)
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Review of Annual General Contract Between Lab and In-house Customer (Clause 7.1)
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Appointment Letter for Technical Manager
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Calibration Review Certificate
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Internal Audit Checklist and Observation Sheet
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List of Procedures
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List of Reference Standards for Verification of Instruments
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Plan for Replicate Retest
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Policy Statement on Chemical Management
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Risk Analysis Register for Laboratory
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Risk Analysis Register for Impartiality
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Undertaking for Maintaining Confidentiality – Non-Disclosure Agreement (NDA)
Uncertainty Excel Sheets (Download)
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Lab Equipment Uncertainty Excel
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Profile Projector Uncertainty Format
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Uncertainty Format for Mechanical and Chemical Testing Labs
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Pressure Measurement Uncertainty Format
Implement 5S System in your Lab
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What is 5s?
02:34 -
Terminology
01:35 -
Pre-Implementation Activity
04:15 -
Zone Segregation
11:30 -
Kick Start Meeting
01:10 -
5s Pledge
02:11 -
1st S Implementation
06:48 -
Red Tag Method
05:12 -
Set in Order (Seiton)
06:51 -
Audit Form Design
04:38 -
Shine (Seiso)
01:56 -
Checklist
02:18 -
Audit Form Design
01:56 -
Standardize (Seiketsu)
01:45 -
Implement Standardize (Seiketsu)
03:01 -
Design Form
01:32 -
Sustain (Shitsuke)
03:35 -
Audit Form Design
04:26
Student Ratings & Reviews
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Good content in general, it will be great if you can add subtitles
