Updated CE Marking Process & ISO 13485:2016 Expectations
Training
Online
*Indicative price
Original amount in USD:
$ 150
Description
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Type
Training
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Level
Advanced
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Methodology
Online
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Class hours
2h
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Duration
1 Day
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Start date
October
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Virtual classes
Yes
Upon completion of this course, attendees will have enhanced knowledge of the ever-changing landscape of Medical Device Regulation in the EU
Facilities
Location
Start date
Start date
Reviews
Subjects
- Medical
- Medical training
- Education
- Training
- Compliance Trainings
- Compliance Management
- Online Courses
- Online Trainings
- Knowledge
- Medical Device
Teachers and trainers (1)
Adam Fleming
Event Manager
Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. . Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements.
Course programme
Learning Objective:Upon completion of this course, attendees will have enhanced knowledge of the ever-changing landscape of Medical Device Regulation in the EUThe 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
Areas Covered in the Session:EU Regulatory and Legislative StructureEU Definition of a Medical Device3 EU Directives -> 2 EU RegulationsKey Agencies InvolvedWhy the change from Directives to Regulations?Overview of CE Marking Process & Changes Resulting from the EU MDRUpdated Role of the Notified BodyMedical Device Classifications
Who Will Benefit:Quality AssuranceRegulatory AffairsClinical Research and Medical OperationsProduct DevelopmentManufacturing / DistributionMedical Device R&DClinical Trial Supply
Speaker Profile:Robert J. Russell For the past 9 years, He has been President of RJR Consulting, Inc. The company assists the pharmaceutical, medical device and biotech industries in understanding and complying with International Regulations affecting compliance, new product development, manufacturing and quality assurance.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: support@compliance4All.com
Additional information
Updated CE Marking Process & ISO 13485:2016 Expectations
*Indicative price
Original amount in USD:
$ 150