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Best Practices for Compliance with FDA 21CFR1040 - 2016
26 Apr 2016
Webinar
Home
Best Practices for Compliance with FDA 21CFR1040 - 2016
Description
Topics
Develop and document the test results in a meaningful report
Develop and document a quality checklist that represents the safety features of the tested system
Learn FDA requirements on GMP training for the tested system
Who should Attend
Laser Safety Officers
Laser System Manufacturers
Laser Importers
Laser Integrators
Engineering Managers
Purchasers of Laser Systems
Contact Officials
Safety Managers
Speaker Profile
Past Events
Best Practices for Compliance with FDA 21CFR1040 - 2016 - 26 Apr 2016, Webinar
(58870)
Important
Please, check "Best Practices for Compliance with FDA 21CFR1040" official website for possible changes, before making any traveling arrangements
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Government & Global Issues:
Law & Regulations
Health & Medicine:
Medical device, Medical technology
Technology:
Equipment & machinery, Optics
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