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此項培訓的目標是培養企業幹部具備對食品過敏原風險規劃與執行管理的能力，並學習如何在產品製造中分類與管制，透過案例演練使學員能掌握食品安全之重要風險管理, 以協助企業持續改善。原價NT$4,000，網路優惠價NT$3,800

The aim of this course is to provide learners with the knowledge and skills required to perform first, second and third-party audits of FSMS against FSSC 22000 v7, in accordance with ISO 19011, ISO/TS 22003 and ISO/IEC 17021, as applicable.Learners who complete this CQI and IRCA Certified FSSC 22000 Lead Auditor Training course successfully (within the five years before making an application to become a certificated auditor) will satisfy the training requirements for initial certification as an IRCA FSMS auditor (Part 1) or IRCA FSMS certified auditor (Part 2) of the scheme. For the full requirements, please refer to quality.org/IRCA-grades.Recommended Prior KnowledgeKnowledge of the following food safety management principles and concepts:The Plan, Do, Check, Act (PDCA) cycleThe core elements of a management system and the interrelationship between top management responsibility, policy, objectives, planning, implementation, measurement, review and continual improvement.Food safety management:Knowledge of the principles of food safety management including pre-requisite programmes as specified in ISO 22000:2018 / TS 22002 (all parts) and HACCP;The relationship between food safety management and the provision of food safe products to prevent or minimise adverse effects on human health and the proactive improvement of food safety performance;Awareness of common examples of relevant national and local FSMS legislation and requirements.Knowledge of the requirements of FSSC 22000 v7 or acceptable equivalent, and the commonly used food safety management terms and definitions, as given in ISO 22000:2018, which may be gained by completing a CQI and IRCA certified ISO 22000:2018 (FSMS) training course or equivalent.Enrolment informationBy enrolling on this course you agree to your personal information being passed to CQI and IRCA.Trusted FSSC 22000  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

ISO 27701:2025 是國際標準組織所發行、專屬於隱私資訊管理的標準。最新版本於 2025年 10月正式公布，持續提供企業組織在蒐集、處理或儲存個人資料時的管理機制設計指引。本標準同時兼顧隱私資訊管理，及有關資訊安全管理的雙重風險評估與控制，促進隱私資訊管理成效。已經取得ISM 27701:2019主導稽核員資格的學員，可透過本課程迅速掌握新舊版本間的差異，輔以隱私資訊管理實務的強化訓練，進一步促進隱私資訊管理系統管理相關工作原價NT$10,000網路優惠NT$9,500

培訓企業幹部具備規劃與執行食品安全防護管理的能力, 透過教學課程了解食品防護與生物恐怖攻擊內容, 強化對食品安全防護管理之要領。原價NT$4,000，網路優惠價NT$3,800

化粧品GMP-優良製造規範指引的國際標準ISO組織於2007年11月15日正式公告發行。此份指引試圖提供與化粧產品有關的優良製造規範指引。此份指引的準備已考量化粧品產業及其特定需求而制定。本指引提供相關組織與實務上會影響產品品質的人員、技術及行政管理層面的建議。是目前ISO組織發行的化妝品指引，最重要的參考。原價NT$4,800，網路優惠價NT$4,560

化粧品GMP-優良製造規範指引的國際標準ISO組織於2007年11月15日正式公告發行。此份指引試圖提供與化粧產品有關的優良製造規範指引。此份指引的準備已考量化粧品產業及其特定需求而制定。本指引提供相關組織與實務上會影響產品品質的人員、技術及行政管理層面的建議。是目前ISO組織發行的化妝品指引，最重要的參考。原價NT$6,000，網路優惠價NT$5,700

本課程旨在協助主管培養教練式領導的核心能力，透過GROW模型（Goal, Reality, Options, Will）的實踐，有效引導團隊成員自我探索、釐清目標並突破瓶頸。課程內容涵蓋教練式溝通技巧，並教導學員如何運用GROW模型，系統性地與部屬進行深度對話。學員將學會設定清晰可衡量的目標，激發成員內在動機，最終提升團隊績效與個人成長，打造高效能的組織文化。原價NT$5,000，網路優惠價NT$4,750特色效益:實務導向，即學即用： 課程不只講述理論，更透過大量的案例分析與分組演練，讓學員能實際操作，並在講師的即時回饋下，內化教練式溝通技巧。工具化與系統化： 課程以GROW模型為核心，提供一套清晰、可依循的對話框架，讓主管在面對不同情境時，都能有系統地引導部屬，而不是憑感覺或經驗行事。情境式教學： 課程會將教練技巧應用於多種真實工作情境中，例如：新進同仁輔導、績效面談、員工激勵與職涯發展等，讓學員知道在什麼時候，該運用什麼技巧。本課程將於結束後授予「上課證明」。

隨著資源日益稀缺與氣候變遷壓力加劇下，線性經濟模式逐漸走向終點，循環經濟已成為各國政策與企業轉型的核心方向。在實務層面上，資源再生、減廢設計與產品可持續性等議題，已逐步納入ESG策略與永續揭露框架中。然而，當前企業所面臨兩大挑戰：其一，缺乏整合性的執行架構，導致行動零散且缺乏協同；其二，是難以量化資源流動與執行成效，使得績效評估與具體目標設定困難，造成實務行動與策略目標之間產生落差。國際標準化組織（International Standardization Organization, ISO）於2024年正式發布ISO 59000系列標準，提供一套具體可行的制度架構，提供制度化的循環經濟推動框架，涵蓋原則、行動、指引、模式與量測等重要面向，提升組織整體轉型效益與可持續性。

This course is certificated by the Chartered Quality Institute and International Register of Certificated Auditors (CQI/IRCA; Course Certification Number, 2428 - PR 369)Course Criteria - ObjectivesUpon completion of this course, learners will be able to:Explain the purpose of a medical device quality management system (MD QMS), interaction with appropriate medical device regulatory authority requirements, quality management systems standard, third-party certification, and the business benefits of the quality management system;Explain the role and responsibilities of an auditor to plan, conduct, report and follow-up a quality management system  in accordance with ISO 19011 (and ISO 17021 where appropriate);Plan, conduct, report and follow-up an audit of a medical device quality management system to establish conformity (or otherwise) with ISO 13485 and applicable medical device regulatory requirement documents in accordance with ISO 19011, ISO/IEC 17021.Learners will need to demonstrate acceptable performance in these areas to complete the course successfully.Prior knowledge Before starting this course, learners are expected to have the following prior knowledge:ISO 13485Knowledge of the requirements of ISO 13485, which may be gained by completing a CQI and IRCA Certified MD QMS ISO 13485:2016 Foundation (FD 132) course or equivalent.Medical Device management System AuditThe Plan, Do, Check, Act (PDCA) cycle.The relationship between ISO 13485 and applicable international regulatory requirements for medical devices.Commonly used quality management terms and definitions within ISO 13485 and ISO 9000.The process approach used in MD QMS.A working knowledge of medical device regulatory process applicable to countries the course is designed to cover, including device regulations, regulatory auditing standards and their relationship with ISO 13485.  This knowledge may be gained by successfully completing a CQI and IRCA course relating to individual regulatory authority standards, which will be available subject to demand (e.g. MD QMS Comprehensive EU Medical Device Regulation 2017/745 (EU MRD) Practitioner - PT 219)A working knowledge of risk management principles related to the design of a medical device, for example ISO 14971

能源是組織運營的關鍵不可缺的要素。 ISO 50001改變了組織管理能源的方式，提供了一個系統化的方法和持續改善的結果，而認知到能源可以被管理和控制是很重要的。此標準既具備作為能源策略管理最佳實踐模式的價值，也具備作為氣候變遷和清潔能源行動基石。藉由提高能源績效和優化能源使用，將有助於降低組織的能源成本。依據 ISO 統計證據顯示，導入 ISO 50001 標準的組織能源改善效益至少為10％ 或更多，最主要是通過低成本或無需投入成本的改善行動，實現節約成本。本課程將介紹新版ISO 50001:2018標準條文運作架構、要求及詮釋案例，以利學員精準解讀能源管理系統標準新版的要求。原價NT$5,000，網路優惠價NT$4,750

與PMI®專案管理手法不同，敏捷開發更加強調滿足客戶價值、漸進式的產品交付模式，以面對需求不確定、快速交付的專案要求。本課程以兩天的實戰課程，融合敏捷開發的基本原則、Scrum操作流程、僕人式的領導等三種元素。帶入企業典型的開發案例，搭配有趣活潑的互動實務演練(Workshop)，引導參訓學員體驗敏捷開發的整體架構，遊戲中學敏捷。 PMI and PMP are registered marks of the Project Management Institute, Inc‧原價NT$12,000，網路優惠價NT$11,400