本课关于单篇微信文案的具体写作技巧、排版技巧等，重点提高具体写作和运营能力。

• 2020-05-29 | 09:00 - 16:00
• Online (webinar link will be shared prior to the event)

The IP Tribunal of the Supreme People’s Court (SPC) recently issued a decision in Dunjun v. Tengda ((2019) SPC IP Civil No. 147), holding that the manufacturer’s making and selling of routers directly infringed a telecommunication method-of-use patent even though the manufacturer itself did not perform the patented method. This case is recognised the Chinese Akamai case.

The European Chamber is delighted to invite Mr. Steve SONG, Partner and Patent Attorney of Beijing DHH Law Firm, who represented the defendant in this landmark case to provide our members insights by studying the judgement of a few cases regarding multi-party patent infringement.

• 2020-05-29 | 14:30 - 16:20
• Zoom online meeting

本课讲微信公众号的整体策划、管理和运营技巧，重点提高整体策划能力。

• 2020-05-28 | 09:00 - 16:00
• Online (webinar link will be shared prior to the event)

The European Union Chamber of Commerce in China together with the European Business Organisation World Wide Network (EBO WWN) is proud to invite you for a special webinar, dedicated to the impact of COVID-19 on the regional economies and business environment.
Experts from each country will provide an update of the evolving COVID-19 situation impacting the markets in their country and the current economic outlook.

What you will learn:
How will the COVID-19 containment and mitigation affect growth, trade and economic outlook in each country?
What are the government strategies to help businesses?
When will market sentiments start to improve?
How can businesses brace for more Covid-19 waves.

Get a baseline view and answers to your questions from our experts, speaker and panel members.

• 2020-05-27 | 10:30 - 12:00
• Online - WEBEX Platform

The Agriculture, Food and Beverage, Cheese, FSMP and PN Working Groups are delighted to invite you to attend a working group meeting on Pest Control in Companies, which will take place on Wednesday, 27th May 2020, from 16:00 to 17:30 in our Shanghai offices as well as on Zoom platform. Please notify your participation method while registering since the office capacity is limited considering the "social distance".

• 2020-05-27 | 16:00 - 17:30
• European Chamber Office Shanghai

Medical resource shortages are increasingly challenging for many countries battling the COVID-19 pandemic. In response to the need, various companies are donating money, personal protective equipment (PPE), ventilators, medicines, disinfectants, food, and other valuable resources. Compliance risks should be carefully considered when providing this valuable assistance to ensure that the resources are put in the right hands with no strings attached. Meanwhile, during the COVID-19 outbreak, the government offers various subsidies to support foreign businesses. Government subsidies beneficiaries face the potential risk of non-compliance.

The European Chamber is delighted to invite Simon Hui, Lead Partner of Baker & McKenzie LLP to share his experience and insights to help our member companies to stay compliant during this special time. The meeting will cover the below topics:

1. Overview of legal requirements under PRC Law
2. Regulatory framework under FCPA, UKBA and France Sapin II Law
3. Industry specific requirements in the medical industry
4. Identify and manage risks arising from donation and government subsidies
5. Case study

Agenda

15:00 – 15:05 Opening by chamber representative
15:05 – 16:00 Presentation by Mr. Simon Hui, Lead Partner of Baker & McKenzie LLP
16:00 – 16:30 Q&A Session

• 2020-05-26 | 15:00 - 16:30
• European Chamber Shanghai Office & Zoom Online Meeting

Mind mapping is a highly effective way of getting information in and out of your brain. Mind mapping is a creative and logical means of note-taking and note-making that literally "maps out" your ideas.

• 2020-05-22 | 09:30 - 15:30
• Online Zoom (webinar link will be shared prior to the event)

In recent years, there is an increasing array of issues related to the field of cybersecurity, data and cloud servicing that are having a very significant impact on the Banking industry. The purpose of this meeting is to shed light into some of these problems, the current regulatory framework, the impact on foreign banks, ways to improve the situation and discuss what banks can do to mitigate some of the problems.

• 2020-05-20 | 09:00 - 10:40
• Online - Zoom (Link to be sent upon confirmation/registration)

The Shanghai Chapter of the European Chamber is pleased to invite CFOs to the next roundtable “China’s Credit Rating System: What CFOs Need to Know”, which is taking place on Wednesday, 20th May, 3:30pm to 4:30pm (GMT+8, China time), via Zoom.

• 2020-05-20 - 2020-05-20 | 15:30 - 16:30
• Zoom

ISO 13485 "Medical Device Quality Management System-Requirements for Regulations" is a quality management system standard for the international medical device industry. Since the upgrade was launched in 2010, after 6 preparations and comments, the new standard has been officially released on March 1, 2016. The new standard incorporates feedback from the medical industry, global experts and competent authorities. BSI, as the UK national standards body and the world's leading announcement body, participated in and provided technical input for the upgrade process.
The new standard adds a large number of best practices in the medical device industry and is compatible with the requirements of national medical device regulations including the US FDA, Japanese JPAL and Brazilian ANVISA GMP. The new standard can help improve the independent research and development capabilities of devices, ensure the safety and effectiveness of medical devices, and enhance the competitiveness of medical device companies.
This course is designed for medical device industry personnel. Participants will fully understand the requirements of the ISO 13485: 2016 quality management system and understand the ISO 14971: 2009 standard-"Relevant concepts of risk management in medical devices".
In-depth understanding of audit principles and how to apply ISO 19011: 2002 standards to perform effective internal audits through group activities, audit exercises, interactive discussions, and coaching courses.


ISO 13485《医疗器械质量管理体系-用于法规的要求》是国际医疗器械行业的质量管理体系标准。自 2010 年启动升版以来，经过 6 的准备和征求意见， 新标准已经于 2016 年 3 月1日正式发布。 新标准融入了医疗行业、全球专家和主管当局的反馈意见。 BSI 作为英国国家标准机构，以及全球领先的公告机构，全程参与并提供了升版的技术输入意见。
新标准增加了大量医疗器械行业最佳实践，兼容了包括美国 FDA, 日本 JPAL 和巴西ANVISA GMP 等国家医疗器械法规的要求，是一部将质量管理体系和法规注册及监管更加紧密结合的标准。新标针对设计和研发等要求可以帮助提升器械自主研发能力，并保证医疗器械的安全有效，从而提升医疗器械企业的自身竞争力。
本课程专为医疗器械行业人员而设。 学员将全面理解 ISO 13485:2016 质量管理体系的要求并了解 ISO 14971:2009 标准——“风险管理在医疗器械的应用的相关概念”。
通过小组活动、审核演练、互动讨论和教练式课程等方式深入理解审核原则和如何应用ISO 19011:2002 标准来执行有效的内审。

参加对象：
• 质量部经理
• 法规部经理

• 2020-05-18 - 2020-05-19 | 09:00 - 17:00
• Online - Zoom Platform