Welcome to SGS Academy

儀器之計量與量測問題與每個人日常生活息息相關，凡是牽涉到交易與買賣，安全與法規要求，學術與研究，服務與品質要求，無一不與量測校正管理相關。計量制度及量測標準的差異卻經常造成交易的障礙，因此各供應商必須制定一套適宜的量測標準與制度，達到與供應鏈及國際顧客量測一致性之要求。SGS率先導入量測法規標準，藉由 ISO9000、ISO10012、ISO17025乃至 ISO14253、ISO GUM1995 之管理標準，以系統思考的角度建構一套量測與校正系統工具，課程包含實驗與理論的依據，以及各種科學與技術領域之各個不確定度的測定及誤差來源分析。SGS校正暨量測實驗室獨自發展以Tolerence & Resolution兩參數運用 R/T Ratio ，導出Mpk量測能力指標提供簡易及安全的量測校正解決方案。課程由淺入深的設計，帶領學員由摸索到實務應用，俾使儀器校正與量測作業達成最佳化。原價NT$3,000

面對新版 ISO 22002 系列標準正式發布，食品業者必須迅速理解「前提方案（PRPs）」如何與食品安全管理系統銜接。本課程以新版 ISO 22002-100:2025 （食品鏈通用前提方案）及 ISO 22002-1:2025 （食品製造業前提方案）為主軸，完整解析條文架構、變更重點與實務應用。課程將帶領學員了解新版條文的主要變化與核心重點，從架構調整、風險思維到永續生產模式要求，幫助企業重新檢視現有前提方案的落實與有效性。原價NT$4,000，網路優惠價NT$3,800

儀器之計量與量測問題與每個人日常生活息息相關，凡是牽涉到交易與買賣，安全與法規要求，學術與研究，服務與品質要求，無一不與量測校正管理相關。計量制度及量測標準的差異卻經常造成交易的障礙，因此各供應商必須制定一套適宜的量測標準與制度，達到與供應鏈及國際顧客量測一致性之要求。SGS率先導入量測法規標準，藉由 ISO9000、ISO10012、ISO17025乃至 ISO14253、ISO GUM1995 之管理標準，以系統思考的角度建構一套量測與校正系統工具，課程包含實驗與理論的依據，以及各種科學與技術領域之各個不確定度的測定及誤差來源分析。SGS校正暨量測實驗室獨自發展以Tolerence & Resolution兩參數運用 R/T Ratio ，導出Mpk量測能力指標提供簡易及安全的量測校正解決方案。課程由淺入深的設計，帶領學員由摸索到實務應用，俾使儀器校正與量測作業達成最佳化。原價NT$3,000

課程介紹VDA 6.5 標准的起源可以追溯到德國汽車工業協會（VDA，Verband der Automobilindustrie）所制定的一套適用於汽車產業供應鏈的產品品質稽核的管理標準，是針對汽車行業中的產品及服務進行稽核和品質管理的要求。是一個在汽車供應鏈中應用的品質稽核標準，旨在保證製造過程中的產品符合要求，並確保產品的品質得到有效控制。VDA 6.5 是開發以產品風險為關注焦點的品質方法，以作為產品生命週期品質風險監控的汽車標準。針對德國汽車行業的產品稽核進行了完整規範。透過課程的闡釋與演練，可讓學員充分瞭解德國汽車工業VDA 6.5產品稽核流程從規劃、抽樣、進行量測、檢驗、最後透過QKZ的判定來理解企業如何應用VDA 6.5 自我檢視產品並且滿足客戶CSR 規定的要求。同時，課程當中講師也會充分說明VDA 6.5 與IATF 16949內部稽核中的產品稽核的差異性，以及VDA 6.3 和VDA 6.5 的差異性與互補性。

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.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 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

隨著數位醫療、遠距醫療、AI醫療軟體（SaMD）、雲端醫療平台及智慧醫療器材快速發展，病患個人資料與健康資料的蒐集、傳輸、儲存及使用已成為全球監管機關高度關注的議題。歐盟《一般資料保護規則》（GDPR）與美國《健康保險可攜與責任法案》（HIPAA）為目前全球最具影響力之個人資料與健康資訊保護法規。醫療器材製造商、醫療軟體開發商、醫療服務提供者及相關供應商，如涉及歐盟或美國市場，皆需了解並建立符合法規要求之資料保護管理機制。本課程將深入解析GDPR與HIPAA的法規架構、核心要求、資料主體權利、資訊安全管理措施及資料外洩通報要求，並結合醫療器材產業實務案例，協助學員建立法規遵循能力與風險管理觀念。課程原價：NTD16,000(含稅)；網路優惠價：NTD15,200(含稅)

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

ISO 50001已於2018年公告新版，更加強調透過能源績效指標(EnPI)及能源基線(EnB)展現企業能源績效持續改善之成果，但如何選擇能源績效指標及建立、維持適切之能源基線，往往也是企業推行能源管理系統人員最頭痛的問題。本課程針對ISO 50001:2018新版能源績效指標及能源基線之相關要求進行深入剖析，讓學員瞭解何謂相關變數、固定因子，如何設定能源績效指標(EnPI)、訂定能源基線(EnB)，以及如何有效運用此兩項工具讓管理作為轉換為實質量化之成效，展現企業在能源管理上持續改善之努力。原價NT$5,000，網路優惠價NT$4,750

為了避免車載資安事故頻傳，導致企業組織的有形與無形損失，歐洲汽車產業制定了TISAX標準，讓汽車產業的廣大供應商遵循此資訊安全管理標準。對於企業高層人員而言，取得TISAX標章，可視為進入汽車產業的重要任務之一；本課程目標為培養具備稽核TISAX能力之專業人才，深入了解標準要求，並透過Workshop演練，實地模擬並磨練稽核技巧，成為具備專業能力的主導稽核員人才。效益‧ 本主導稽核員課程以TISAX ISA6.0指導有效帶領TISAX稽核和審查時所需之  技巧及知識，詳細解說TISAX獨立稽核的原則及實際作業情形，藉由分組活  動逐步引導參加者學習從管理稽核規劃到報告稽核結果的整體過程。課程包  含角色演練、小組研習及公開討論時段。‧ 參加全程課程者授予「上課證明」，參加全程課程並考試通過者，授予  SGS「成功修業證書」。原價NT$48,000網路優惠價NT$45,600

本課程以「食品安全 × ESG × 經營治理」為主軸，協助企業將分散的管理制度，整合為可運作的永續治理架構，讓企業看見制度與現場落差的真正原因。協助高階主管理解ESG如何影響企業長期營運與品牌，同時降低食品安全事件機率及強化品牌信任。原價NT$5,000，網路優惠價NT$4,750