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Combination Products Registration 2017
10 Jul 2017
Webinar
Home
Combination Products Registration 2017
Description
Topics
CE Marking
EU/US
Documentation requirements for combination products EU/US
510 K and PMAs general Overview
Managing third parties and document control
Interfacing,Development,Quality,Regulatory
Vigilance and adverse event reporting
Who should Attend
Medical Officers
Regulatory Affairs
Past Events
Combination Products Registration 2017 - 10 Jul 2017, Webinar
(68186)
Important
Please, check "Combination Products Registration" official website for possible changes, before making any traveling arrangements
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