Updated CE Marking Process & ISO 13485:2016 Expectations

  • 150.00 Dollar US$
  • Published date: May 23, 2019
    • Fremont, California, United States

Overview:
After completion of this course, attendees will have enhanced knowledge of the ever-changing landscape of Medical Device Regulation in the EU.

Learning Objective:

Upon completion of this course, attendees will have enhanced knowledge of the ever-changing landscape of Medical Device Regulation in the EU.

The content of this course is designed to simplify the understanding of requirements and to provide attendees with the latest insight on how changes are being viewed and implemented by companies marketing products in the EU.

Who Will Benefit:
Quality Assurance
Regulatory Affairs
Clinical Research and Medical Operations
Product Development

Speaker Profile:

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com

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Compliance4All
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