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Xtalks Life Science Webinars, Online
2016-05-04
Key Topics will Include: - Useful tips for developing validation studies that are accepted on the first submission
- How to properly classify your device for reprocessing
- Understanding FDA’s six criteria for reprocessing instructions
- Understanding cleaning, disinfection, and sterilization – the differences between them and how they should be applied to products based on classification
- Useful tips on developing Instructions for Use to minimize human error or confusion
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Organized by:
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Xtalks Life Science Webinars |
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Invited Speakers:
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Steven Elliott, Director, Quality Control and Sterility Assurance, NAMSA
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Deadline for Abstracts:
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2016-05-04
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Registration:
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Free
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E-mail:
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helpdesk@xtalks.com
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