IoPP Standard Webinar: “The Do’s and Don’ts of Sterile Medical Device Packaging"
 
To be compliant with ISO 11607 part 2, medical device companies must have a validation program to demonstrate repeatability and reproducibility of the sealing process. As the FDA continues to regulate the processes involved in medical sterile packaging systems, the need for reducing variation on these processes becomes more critical. 
 
What you will learn:
  • How to reduce process variation by having better equipment designs
  • How to establish the right sealing pressure for a specific package
  • How to establish a calibration method that does not affect process outcome
Even if you’re not a packaging professional working in medical devices, this webinar may include a useful takeaway or two for you.
 
Speaker:
Charlie Rivera, CPP
Corporate Packaging Operations Manager
 
Where:
Online
 
When:
November 11, 2014
2:00 p.m. – 3:00 p.m. CST
 
Costs:
IoPP Regular, Premium and Elite Membes: FREE
IoPP Affiliates and Non-Members: $99
 
Click here to register for the webinar.
 
Sponsored by:
 
 
Supported by:
 

 
 
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