Webinar on Medical Devices Designing with Cleanliness in Mind
Website https://compliancetrainings.com/product/medical-devices-designing-with-cleanliness-in-mind-9/ |
Category Clinical & Laboratory, FDA Compliance, Food, Drugs & Biologics, Information Technology, Medical Devices
Deadline: January 31, 2017 | Date: January 31, 2017
Venue/Country: Online, Canada
Updated: 2016-12-19 22:33:41 (GMT+9)
Call For Papers - CFPCleanliness is a hot topic in the medical device industry. The FDA expects medical device companies to validate the cleanliness of their devices. One of the best ways to achieve a clean device is by designing it with cleanliness in mind.This 60 minutes webinar will provide in-depth and valuable guidance to medical device manufacturers on design considerations for both single-use and re-usable devices. There are certain design elements that are more difficult to clean and should be avoided whenever possible. With the “right” design, both the manufacturing and cleaning processes can be simplified.Areas Covered in the Session :Design RequirementsSingle-Use Design ConsiderationsRe-usable Design ConsiderationsDesign Elements to Avoid/MinimizeSimplifying the Manufacturing ProcessSimplifying the Cleaning ProcessWho Will Benefit:QA/QC managers and personnelValidation managers and personnelR&D and EngineeringManufacturers of Implantable Medical DevicesManufacturers of Single-Use Medical DevicesManufacturers of Reprocessed/Reusable Medical Devices
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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