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VILAS

VIAS

VICAS

VILAS Med

VIPAS

VIRAS

GLP-OECD
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VIPAS

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GLPOECD

TẤT CẢ KHÓA HỌC

1. ISO/IEC 17025:2017 Standard
2. Quality assurance of testing/calibration results
3. Laboratory management skills
4. Skills for internal auditors in laboratories
5. Selection and validation of test methods
6. Risk Management in Laboratory Operations
7. Decision Rule Implementation
8. Developing a Laboratory Management System Documentation
9. Evaluation of measurement uncertainty
10. Internal Auditing for Laboratories
11. Professional Skills of Lead Assessors in Laboratory Evaluation

1. ISO 15189:2022 Standard
2. Developing quality management system documents
3. Selection and validation of diagnostic methods
4. Measurement uncertainty for medical laboratories
5. Internal auditing for medical laboratories
6. Ensuring and validity of examination results
7. Risk management

1. QMS Certification System – based on ISO/IEC 17021-1/3
2. EMS Certification System – based on ISO/IEC 17021-1/2
3. FSMS Certification System – based on ISO/IEC 17021-1 and ISO 22003-1
4. MDMS Certification System – based on ISO/IEC 17021-1 and IAF MD9
5. Product Certification System – based on ISO/IEC 17065
6. Greenhouse Gas Validation and Verification System – based on ISO/IEC 17029:2019, ISO 14065:2020, ISO 14066:2023, ISO 14064-3:2019, and IAF MD6:2023

1. ISO/IEC 17020:2012 and VIAS policies
2. Internal audit of an inspection body according to ISO/IEC 17020

1. ISO/IEC 17043:2023 Standard

1. ISO 17034:2016 Standard

1. Introduction to OECD GLP Requirements
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Biotechnology Testing Laboratory