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

The importance of the ability to solve problems has increased at the same rate as the pace of economic and technological change in recent years. The only way to successfully navigate through these changes is to be a fluent and creative problem solver. That's why the World Economic Forum has identified complex problem solving as the most important skill for the twenty-first century.

• 2022-12-16 | 09:00 - 17:00
• KIT China Branch

Nowadays, with the rapid change of customer needs and requirements, manufacturing enterprises must gradually adjust their traditional manufacturing to flexible production, in order to meet the increasing customer expectations. Flexible production is characterized by variety, small batch, the shortest delivery time and the best quality. In addition, with the increasing price of land and labor in China, manufacturing enterprises are facing increasing internal and external pressure to maintain their competitiveness in the market. Lean factory planning is a starting point for the overall improvement of manufacturing enterprises. It lays a solid foundation for lean improvement of enterprises from the macro layout and is an important premise for micro-lean improvement and intelligent manufacturing in the future.

• 2022-12-16 | 09:00 - 17:00
• Bomag Changzhou Plant

以下是12月线上课程安排
The online class schedules in December are listed below.

- 企业节能与可再生能源项目的识别、设计及减排评估 Identification, design and carbon mitigation assessment for industrial energy efficiency and renewable energy projects
- 可持续发展管理体系与ESG评级 Sustainable development management system and ESG rating
- ISO13485 医疗器械行业质量管理内审员 ISO13485 Internal Auditor
- 可靠性工程 Reliability Engineering
- 欧盟新医疗器械法规之MDR EU Medical Device Regulations
- ISO/IEC 17025:2017实验室体系内审员 ISO/IEC 17025:2005 Internal Auditor
- 管理者多角度思维 Managers - Multi-angle System Solving Problems

• 2022-12-15 - 2022-12-23 | 09:00 - 22:00
• Guangzhou

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

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
• Zoom online

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

The new EU Medical Device Regulation MDR (EU)2017/745, which replaces the previous MDD (93/42/EEC) directive and AIMD (90/385/EEC) directive, entered into force in May 2017 and became mandatory in May 2021. Compared with the current medical device directive, MDR adds many new regulatory requirements, such as the requirement of unique device identification (UDI), the requirement of regularly updating CE technical documents, and the requirement of post-market supervision. The transition period of MDR is very short, and this change is bound to have a significant impact on relevant Chinese medical device enterprises, which requires active response. This course provides guidance for organizations upgrading from MDD to MDR certification to customize and implement an independent CE conversion plan.

新的欧盟医疗器械法规 MDR (EU)2017/745 取代了之前的 MDD（93/42/EEC）指令和 AIMD（90/385/EEC）指令，已于 2017 年 5 月生效，并于 2021 年 5 月强制实施。相比现行医疗器械指令而言，MDR 增加了很多新的法规要求，比如：唯一器械标识（UDI）的要求、定期更新 CE 技术文件的要求、上市后市场监督的要求等。MDR 过渡期时间很短，此次变更势必对相关中国医疗器械企业造成重大影响，需要积极应对。此课程为 MDD 升级到 MDR 认证的企业提供指导，定制一套独立的 CE 转换计划并有效实施。

• 2022-12-12 - 2022-12-15 | 09:00 - 17:00
• Online Training