Upcoming Events

由于关系到人类本身的健康和安全,全球对医疗器械行业都有严格的要求。在欧洲市场上,医疗器械生产厂商早已被强制要求通过认证机构的CE认证。市场的压力使国内医疗器械企业深入了解这方面的要求成为迫切的需要。本课程将透彻的讲解医疗器械行业认证要求,使您全面掌握有关ISO 13485:2016的相关要求,有效的进行体系内审工作。
Due to an increasing global awareness to health and safety issues, higher regulatory requirements have been introduced especially to medical equipment manufacturers. In Europe, medical equipment market pressure has prompted Chinese medical equipment manufacturers to fully comprehend according to these requirements. This course provides clear explanations to the newly introduced relevant requirements outlined in ISO 13485:2016 and will equip participants with the tools to effectively implement internal audits.

  • 2020-02-17 | 09:00 - 17:00
  • TÜV Rheinland Office | 莱茵深圳办公室

As a manufacturing company, the most you concern must be changes and fluctuations in customers demand. Taking the automotive industry as an example, what they most concern: What requirements do OEMs have on us? What can we do to reduce the company’s inventory at the supply chain nodes? What does consignment management mean to us? How can we reduce the risk of consignment inventory and achieve full tracking of consignment inventory? What is the automotive lean supply chain? Can it really help our auto parts companies reduce their inventory?

  • 2020-02-24 | 09:00 - 17:00
  • TÜV莱茵广州office1楼鲁班培训室 | TÜV Rheinland Guangzhou office