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This webinar covers key aspects of ISO 13485:2016, including management responsibilities, document control, design & development, supplier management, manufacturing processes, and corrective & preventive actions. Compliance with this international standard is crucial for medical device manufacturers to access major markets worldwide.
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Timings09:00 AM-06:00 PM (expected)Not Verified | Entry FeesCheck Official Website |
Estimated Turnoutupto 100 Delegates | Event TypeConference |
EditionsMar 2025 InterestedFrequency Newly Listed | Official LinksWebsiteContacts Report Error Claim this event |
Organizer![]() ComplianceIQ USA1524 Total Events • 525 Followers |
EditionMar 2025
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https://10times.com/hub/medical-pharma-hub