This training mainly explains the evolution history of ISO/IEC 27001 standard and the concept of safety management at home and abroad, and combined with years of training project practical experience, 93 security control requirements of ISMS system and how to achieve the incisive description, so that students can master the correct theoretical knowledge and working methods, explanation of system document framework design and system key activities (risk assessment, internal audit, management audit, etc.) as well as pay attention to the ability of the system of internal audit training, the organization of internal audit activities to carry out the method and process of emphasis on explanation. Finally, the framework of information security basic knowledge and working methods has been strengthened for all departments and personnel of the enterprise, and a good foundation has been laid for the ISO/IEC 27001 system construction and the follow-up of information security work.

本培训主要讲解了 ISO/IEC 27001 标准和国内外安全管理理念的演变历史，并结合多年的培训项目实战经验，对 ISMS 体系 93 项安全控制要求以及如何实现进行了精辟的讲述，使学员掌提正确的理论知识和工作方法，此外，对体系文件框架设计和体系关键活动（风险评估、内审、管审等）进行深入说明。同时，关注体系内审员的能力培训，对内审活动的组织开展方法和过程进行重点讲解。最终，为企业各部门和人员夯实了信息安全基础知识和工作方法的框架，为企业 ISO/IEC 27001 体系建设和信息安全工作的后续开展奠定了良好基础。

• 2022-12-29 - 2022-12-30 | 09:00 - 17:00
• Online Training

This course is a 3-day live online course. The aim of this training is to provide participants with a thorough grounding in the ISO 9001:2015 standard, the background to ISO 9001, its requirements and its role for companies. The aim of this training is to provide participants with a comprehensive grounding in the ISO 9001:2015 standard. Through the training, participants will be able to understand the ideas and methods for establishing and improving a quality management system, and be equipped to promote the system, maintain and continuously improve the management system through internal audits and other means. They will have the ability to maintain and continuously improve the management system through internal audits and other means.
本课程为 3 天在线直播课程。此培训的目的是帮助学员了解ISO9001:2015标准的全面基础知识，知晓ISO 9001的背景、条文要求及其对企业的作用。通过培训使学员了解建立和完善质量管理体系的思路和方法，具备体系推进，通过内部审核等手段维护及持续改进管理体系的能力。

• 2022-12-21 - 2022-12-23 | 09:00 - 17:00
• Online webinar

With the deepening of certification, enterprises need a group of internal auditors with good quality and ability of environmental management system. The internal auditor can carry out the internal audit work according to the internal audit procedure, help the enterprise to find the problems in the operation process of the system and improve the environmental management system established by the enterprise, which plays an effective role in promoting the pollution prevention and improvement of the enterprise's performance in environmental management.

随着贯标认证工作的深入，企业需要一批具备良好素养和能力的环境管理体系的内审员。内审员能够按照内审的程序开展内审工作，帮助企业发现体系运行过程的问题并完善本企业建立的环境管理体系，对企业污染预防及改进在环境管理方面的绩效起到有效的促进作用。

• 2022-12-20 - 2022-12-21 | 09:00 - 17:00
• Online Training

FMEA, the most important tool for risk analysis, originated in aerospace and was brought to the automotive industry in the late 1970s. After decades of development, the latest version of FMEA was published jointly by AIAG and VDA in June 2019, giving a structured and logical seven-step FMEA analysis.

FMEA作为风险分析最重要的工具，发源于航空航天，在70年代末被引入汽车行业。经过几十年的发展，最新版FMEA于2019年6月由AIAG与VDA联合发布，给出了结构化、逻辑化的七步FMEA分析法。

• 2022-12-20 - 2022-12-21 | 09:00 - 17:00
• Online training (2 days)

【 Course Objectives 】
● Master Excel using skills, improve the way of work, improve work efficiency;
● Design a pleasing professional data report, using more than three functions nested to solve complex problems;
● Create professional "talking" charts to generate arbitrary reports from Pivottables.

【课程目标】
·掌握 Excel 使用技巧，改善工作方式，提高工作效率；
·设计令人赏心悦目的专业数据报表，通过三个以上的函数嵌套解决复杂工作问题；
·创建“会说话”的专业图表，通过数据透视表随便所欲生成各种报表。

• 2022-12-20 | 09:00 - 16:10
• Online Training

With the continuous development of economy and society, the quality of products has been highly valued by people. The level of laboratory management plays an extremely important role in product quality control, directly affecting the stability of the company's products, quality improvement and the rapid advancement of new products. It undertakes the important tasks of index control and process research and development. Enterprise laboratory management level and technical ability are challenged by more and more customers, requiring more professional testing reports. In order to meet the challenges, the laboratory should accurately grasp the relevant requirements of ISO/IEC 17025 and establish an effective quality management system according to it. It can not only prove its technical ability to the society and customers, but also realize self-improvement of the laboratory, and constantly improve the detection technology ability, shorten the gap with the authoritative laboratory, to adapt to the new requirements of customers.

随着经济社会的不断发展，产品的质量问题受到了人们的高度重视，而实验室管理水平的高低，对产品质量控制起着极为重要的作用，直接影响着公司产品的稳定性、质量改进以及新产品的快速推进，承担着指标控制和工艺研发的重要任务。企业实验室管理水平和技术能力受到越来越多客户的挑战，要求出具更专业的检测报告。为了应对挑战，实验室应准确地掌握 ISO/IEC 17025相关要求，并按其建立有效的质量管理体系。其不仅可以向社会、客户证明自己的技术能力，而且还可以实现实验室自我改进，并不断提高检测技术能力，缩短与权威实验室差距，适应客户不断提出的新要求。

• 2022-12-19 - 2022-12-21 | 09:00 - 17:00
• Online Training

管理者在充满压力的会议中，向领导或者跨部门团队做正式汇报的时候，最大的挑战莫过于如何：

· 切中要害，获取支持

· 逻辑性强，富有条理

· 简明扼要、突出重点

本课程所教授的是，“在汇报中Sell你的想法——以听众为中心的思维模式和叙事逻辑”。

• 2022-12-14 | 09:00 - 16:00
• Online - Zoom training link will be shared prior to the training by email 线上课程 - Zoom培训链接将于会议前发送到报名邮箱

Common problems and misunderstandings of enterprises
·How to relax tolerances scientifically? What are the new tolerance application experiences?
·How to reduce technical disputes and simplify measurement work? So as to reduce the risk of measurement, as well as avoid the occurrence of misacceptance and rejection?
·How to improve the level of research and development, save manufacturing costs, improve the pass rate?
This course is highly practical. Several practical cases (especially classic error cases) are interspersed throughout the training. These cases will guide students to analyze the advantages of GD&T in design, assembly, inspection and application, so that students can understand and learn to apply GD&T.

企业常见问题与误区
·如何科学放宽公差？有哪些新的公差应用经验？
·如何减少技术纠纷，简化测量工作？从而减少测量的风险，以及避免误收和拒收的发生？
·如何提升研发水平，节约制造成本，提升合格率？
本课程实用性很强，将若干实用案例（特别是经典错误案例）穿插在培训中，这些案例将引导学员剖析GD&T 在设计、装配、检测和应用等等方面的优点，让学员理解并学会应用 GD&T。

• 2022-12-12 - 2022-12-13 | 09:00 - 17:00
• Online Training

This training is a 3-day live online training.
The automotive industry quality system standard IATF 16949:2016, developed by the IATF, clearly stipulates that organizations should have qualified internal auditors. This course is specifically designed for organisations implementing IATF 16949:2016 or training for certification purposes. Participants will learn the intent and requirements of IATF 16949:2016, including an introduction to the process approach and its core tools for the automotive industry. Through a precise understanding of the standard requirements, the simulation audit of the application of audit techniques and process methods in the automotive industry, the internal auditors of the organization can master the basic requirements of IATF 16949:2016 and have the ability to plan and complete the internal audit.

本课程为 3 天在线直播课程。
IATF 所制定的汽车行业质量体系标准 IATF 16949:2016 中明确规定，组织应具有有资格的内部审核员。本课程特别为组织推行 IATF 16949:2016 或认证目的培训。学员将学习到 IATF 16949:2016 的意图和要求，包括过程方法及其汽车行业核心工具介绍。通过对标准要求的精准理解，汽车行业审核技巧及过程方法应用的模拟审核，使组织的内审员可以掌握 IATF 16949:2016 基本要求并有能力策划完成内部审核。

• 2022-12-12 - 2022-12-14 | 09:00 - 17:30
• Online webinar

By deeply understanding the content of ISO 13485, this course will deepen the understanding of the specific requirements, risk analysis and evaluation, identification and traceability, feedback system, warning system, advisory notice, etc. related to the safety and effectiveness of medical devices. According to the basic principles of auditing, we can audit the internal quality management system, obtain audit evidence, and conduct a correct and objective audit evaluation of ISO 13485 system from the aspects of meeting the requirements of laws and regulations and maintaining an effective quality management system.

本课程将通过深入了解 ISO 13485 标准内容，加深理解医疗器械所特有的与产品安全性有效性有关的特定要求、风险分析和评估、标识与追溯、反馈系统、警戒系统、忠告性通知等；并能按照审核的基本原则，执行内部质量管理体系审核，获取审核证据，从满足法规要求、保持有效的质量管理体系等方面对 ISO 13485 体系进行正确客观的审核评价。

• 2022-12-12 - 2022-12-14 | 09:00 - 17:00
• Online webinar