***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.***

This course aims to provide learners with the knowledge and skills required to perform first, second and third-party audits of environmental management systems against (EMS) ISO 14001, in accordance with ISO 19011 and ISO 17021, as applicable.Learners who successfully complete this CQI and IRCA Certified Auditor/Lead Auditor (EMS) Training course (within the five years before making an application to become a certificated auditor) will satisfy the training requirements for initial certification as a certified IRCA EMS auditor. For full training and requirements, please refer to quality.org/IRCA-grades.This course is recognised by APSCA for CPD purposes, aligned with the APSCA Competency Framework and is worth 36 CPD credits.Recommended Prior Knowledge Management systemsThe Plan, Do, Check, Act (PDCA) cycleThe core elements of a management system and the interrelationship between top management responsibility, policy, planning, implementation, measurement, review and continual improvementEnvironmental management - The intended outcomes of an environmental management system:Enhancement of environmental performanceMeeting compliance obligationsAchievement of environmental objectivesISO 14001Knowledge of the requirements of ISO 14001 and the commonly used environmental management terms and definitions, which may be gained by completing a CQI and IRCA Certified ISO 14001:2026 Foundation (EMS) (FD135) Training course or equivalent.Enrolment informationBy enrolling on this course you agree to your personal information being passed to CQI and IRCA.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.Trusted ISO 14001 Lead Auditor training from a leading course providerOur courses are delivered by tutors who are environmental management system experts and experienced trainers. Your knowledge and skills will be developed through an interactive and practical approach to learning. Case study materials and role-play exercises are used to develop and practice skills in all phases of auditing. Participants are continually assessed and required to complete an end-of-course written examination.Contact your local SGS office for full details of the courses available in your region.

CONTENT- Introduction to quality and environmental management system.- Concept of development for integrated management system.- Principle to quality management system.- Review the requirement of integrated management system.- Environmental situation and risk management.- Development and practical of integral management system.   Conducting Auditing for Integrated management system

-Concept of internal audit & Hygiene Inspection -Objective of internal audit/hygiene inspection -Conclusion of quality management system for BRCGS PM7-Planning and audit plan -Preparation and internal audit -Internal audit performing -Corrective action/Follow up and Close meeting -Reporting -PDCA Cycle-Paper examination 

***ใบรับรองผลและเอกสารการเรียนการสอนจะอยู่ในรูปแบบข้อมูลอิเล็กทรอนิกส์ (เอกสารการเรียนการสอนอิเล็กทรอนิกส์เฉพาะการฝึกอบรมแบบ In-house)*** *ระบบบริหารคุณภาพ (ISO 9001:2015) เหมาะสำหรับธุรกิจทุกประเภทและทุกขนาดองค์กร*

-What is Food Allergen/Food Fraud/Food Defense? -Update GFSI guidance document  version 2020 and GFSI standard (BRCGS, IFS, FSSC 22000 and SQF) with related food allergen, food fraud and food defense requirements-Step in Developing a Food Allergen , Food Fraud and Food Defense Plan and TACCP/VACCP Assessment 

*** 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.***

ISO 14067 Carbon Footprint of Products: Requirements & Guidelines for Quantification & Communication Course allows the participants to understand how to implement a systematic framework for carbon footprint of products (CFP) study in which organizations drive continual improvement, using a risk-based approach. The course would also help internal and external auditors to understand important aspects in communication and verification of a CFP study.ISO 14067 builds largely on the existing ISO standards which specifies principles, requirements and guidelines for the quantification and communication of the carbon footprint of a product (CFP).Customers, consumers and shareholders are increasingly concerned with the environmental impact of the activities, products and services they are engaged in. This may be seen as a challenge, but it is also an opportunity. Carbon footprint verification from ISO 14067 enables organizations to demonstrate environmental responsibility, stand out from the competitions and demonstrate to the existing and potential customers of its commitment. Organizations can demonstrate its commitment to reducing the impact of its daily operations on the environment with carbon footprint analysis based on ISO 14067 standard.

*** SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables leaners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***The training has been designed to give you the necessary skills to perform internal audits on an organization’s Quality Management Systems (QMS) for Medical Devices to the requirements of to ISO 13485:2016 and to contribute to their continual improvement. This intensive training aims to provide delegates with the skills required to conduct internal audits, using interactive training by medical device lead auditors experienced in ISO 13485 and Notified Body audits.