หลักสูตรทั้งหมด

 ***SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables learners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***CONTENT Organization context in accordance with ISO45001 Risk assessment Hazard identification Action plan for OHS risk control Workshop (for 2-day course)

The reasons why the PECB Certified ISO/IEC 27001 Lead Implementer training course is more desirable and valuable than the others is because it not only enables you to acquire the knowledge and competence in implementing an information security management system (ISMS) but also teaches you how to apply the skills required in practice. In addition to what the ISO/IEC 27001 standard tells you to do, this training course instead tells you how to do it, through various activities, exercises, case studies, multiple-choice standalone quizzes, and scenario-based quizzes. These will allow you to test your knowledge about the implementation process steps. After attending the training course, you can take the exam. The exam type is unique because it is open-book and contains multiple-choice questions. It also contains standalone questions and scenario-based questions, which aim to simulate a real-life situations. If you successfully pass it, you can apply for a “PECB Certified ISO/IEC 27001 Lead Implementer” credential, which demonstrates your ability and practical knowledge to implement an ISMS based on the requirements of ISO/IEC 27001.

This course is certificated by the Chartered Quality Institute and International Register of Certificated Auditors (CQI / IRCA); Course Certification Number, 2142 – PR 366.Learners who successfully complete this programme may be eligible to apply for certification by the CQI / IRCA as an auditor, lead auditor or internal auditor within five years of course completion.Other requirements for certification are outlined in this manual and described on the CQI / IRCA website www.quality.org. 

CQI / IRCA Accreditation We are accredited by the Chartered Quality Institute (CQI) and  International Register of Certified Auditors (IRCA) globally. This course is accredited by IRCA, 1910 - PR 357.This is a Chartered Quality Institute and International Register of Certificated Auditors Certificated Training Course.This course is recognised by APSCA for CPD purposes, aligned with the APSCA Competency Framework and is worth 36 CPD credits.DisclaimerFor learners undertaking the CQI and IRCA Online Assessment, all aspects relating to examination, proctoring, disqualification decisions, appeals and the issuance of results to the Approved Training Partner (ATP) are the sole responsibility of CQI and IRCA. SGS does not have oversight of, or involvement in, these processes.PRIOR KNOWLEDGEBefore starting this course, delegates are required to have the following prior knowledge:Knowledge of the following OHS management principles and concepts:The concept of OHS sustainable development whereby an organisation must ensure that actions of today do not degrade the environment of the future.The purpose of an initial review as the basis for establishing an OHS management system where none currently exists.Evaluation of activities, products and services in order to establish the risks and hazards associated with normal operating conditions, abnormal conditions such as start-up and shutdown and emergency situations and accidents.Considerations of risks and hazards in respect of:workplace locations;workplace activities;work-related activities carried out away from the normal place of work or base;employees, visitors and other interested parties in areas where the organisation has control and influence over health and safety;vulnerable individuals within the workplace or control of the organisation.Occupational Health and Safety legislation and how legal compliance forms part of an OH&S management system.A good appreciation of typical methods for evaluation of risks and hazards and their mitigation and the identification of improvements (e.g., risk assessments and method statements).

CONTENT- บทนาสู่การจัดทามาตรฐานและแนวทางการตรวจร่วม 2 มาตรฐาน- ภาพรวมของข้อกำหนดระบบคุณภาพของทั้ง 2 มาตรฐาน- ประเภทและกลยุทธ์ของการตรวจฯ- การตรวจประเมินตามข้อกำหนดของ ทั้ง 2 มาตรฐาน- การจัดการกับสิ่งที่ไม่เป็นไปตามข้อกาหนด- การรายงานการตรวจติดตาม และการติดตามผล- การตรวจประเมินสู่การพัฒนาอย่างต่อเนื่อง

***SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables learners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***1. Delegates would clearly understand roles and responsibilities of supervisor2. Effective self and team improvement3. Understand and able to plan effectively4. Know how to communicate successfully5. Become knowledgeable in an organizational relationship6. Improve work and team in order to reach maximum job performances

*** SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables learners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***CONTENT Certified of laboratory and Metrological traceability Change of criteria and support documents by Thai Industry Standard Instutite. The quality of the laboratory and the standard structure. ISO/IEC 17025 version 2017 Requirements. Guidelines to comply with the requirements. How to comply with Management System Option A & B. Preparation. Laboratory Sample exercises.

***SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables learners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***To prepare the organization’s understanding of Higg Facility Environmental Module

Implementation of European Medical Device Regulations is the primary requirements while demonstrating the compliance to regulatory requirements while placing the products in European Market for the Medical Device manufacturers and to place CE marking on the products. The European Council Directives 90/385/EEC and 93/42/EEC has been revised to Regulation (EU) 2017/745. European Medical Devices Regulation (MDR), was published in the Official Journal of the European Union on May 5, 2017. The Regulation (EU) 2017/745, covers medical devices and active implantable medical devices.

***SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables learners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***- Changes in new version of ISO/IEC 27001:2022- Introduction to Information Security Management System- Principles of Information Security Management- Risk management based on ISO/IEC 27001 and Risk control for manage Information Security Risks  -Introduce of ISO/IEC 27001:2022 Requirement and Annex A. Controls