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ISO 80369 Standards Bring Changes to Medical Device CompaniesAvailable on Demand
Date: September 12, 2016 – September 12, 2017
Time: 8:00 AM PST | 11:00 AM EST
Duration: 60-minutes
Sponsored by:

About this webinar
As the leading global pharmaceutical component manufacturer, Nordson MEDICAL is excited to sponsor this webinar addressing the details surrounding the new ISO 80369 standards that are affecting medical device manufacturers, specifically for respiratory, enteral, cuff inflation, neuraxial, and IV applications.
Driven by a desire for greater patient safety, the development of these standards will reduce the occurrence of misconnections caused by the inadvertent connection of incorrect systems. Compliance with ISO 80369 standards requires new connector specifications for specific applications, and Nordson MEDICAL will discuss the implications of these changes.
The expert in this webinar will outline the key things you need to know about ISO 80369 standards. Learn what the standards are, how the industry will be affected, when the standards will come into effect, and how to stay up-to-date on ISO 80369 news.
You will Learn:
- What ISO 80369 standards are
- Why the industry needs ISO 80369 standards
- How ISO 80369 standards will affect medical device companies
- When the ISO 80369 standards will come into effect
This webinar will address the details surrounding the new ISO 80369 standards that are affecting medical device manufacturers. The expert in this webinar will outline what ISO 80369 standards are, how they will affect the industry, and when the standards will come into effect.
Speaker:
Jim Skog
Global Market Development Manager
Nordson MEDICAL
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