Recorded Wednesday, July 26 – Presented by Trinseo
Join us as we discuss the importance of medical grade plastic material compliance in end-product safety.
Medical devices are required to be compliant to a series of stringent regulations and selecting the right plastic material is the first step to achieving product safety. In this webinar, we will provide an overview of quality control systems and medical material production and introduce why they are essential for end-product safety. In addition, the following manufacturing systems will be discussed:
– cGMP
– ISO 13485
– ISO 10993 (USP VI)
Join us for insights into how you can improve your chances of medical device application compliance by selecting the appropriate materials upfront. Lastly, hear about the materials that have been developed to satisfy customer needs.
盛禧奥将于7月26日下午3:00 – 4:00（北京时间）进行即时网络研讨会，探讨医疗级塑料的合规性对终端产品安全起到的关键作用。
医疗产品必须符合一系列严格的法规要求，为产品正确选择基础塑料是产品安全的第一步。本次网络研讨会，我们将介绍医用材料制造商的质量管控和生产标准的重要性，以及分析其对医疗产品制造商进行的风险分析和质量监控影响。此外，以下制造管理系统也会一一探讨：
– cGMP
– ISO 13485
– ISO 10993（USP VI）
请涌跃参加我们的网络研讨会，了解如何选择医用材料，从源头来提高医疗产品的合规性。 最后，不忘听听为满足医疗客户需求而开发的材料。
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Webinar Transcript
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