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2019 - Updated CE Marking Process & ISO 13485:2016 Expectations
Date2019-07-12
Deadline2019-07-10
VenueFremont, USA - United States 
KeywordsEU Medical Device Regulation; Single Audit Program; Clinical Research
Topics/Call fo Papers
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-AT-gmail.com
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-AT-gmail.com
Other CFPs
Last modified: 2019-06-14 14:26:51