The Medical Device Summer School - From Concept to CE Marking
Course
In The Rembrandt Hotel, London
Description
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Type
Intensive workshop
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Level
Intermediate
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Location
The rembrandt hotel, london
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Class hours
8h
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Duration
5 Days
A residential rate to include 4 nights accommodation (bed & breakfast), theatre trip and buffet supper is also available when booking. Please contact our operations team if you would like this option on our Contact form.
Benefits of attending this five day course
Understand the Procedures for Taking a Medical Device to the Market Place
Learn what Regulations Control the Manufacture and Marketing of Devices in the EU
Gain an Insight into Different Aspects of the Process for Obtaining the CE Mark for a Device
Discover a Holistic Approach to Device Development and Marketing
Participate in Workshops and Learn from Other People’s Experiences
Understand how Other Professionals Affect the Process for Bringing a Device to Market
Network with Participants from Organisations Similar to Your Own
Bringing a Medical Device to the market place is a complex and lengthy procedure which requires experience, knowledge and specialist skills. The contribution to a successful market placement comes from many different skilled individuals and organisations. Those contributing towards the placing of devices on the market should be aware of all the stages involved and be able to relate their responsibilities to the needs of other professionals, scientists, clinicians and regulatory and quality experts.
Facilities
Location
Start date
Start date
About this course
This comprehensive course has been designed to map the processes from device concept to marketing and show how regulatory, quality, clinical and other aspects of device development are joined into a continuous process. It will commence with a general introduction as to what devices are and how they are developed, and continue with lectures, workshops and case studies covering each process applicable to device development, marketing and eventually the post market procedures. There will be ample time for informal discussions alongside the presentations and workshops.
This course has been designed primarily for those who wish to understand the processes involved in bringing a medical device to market. General medical devices as well as Active Implantable, In-Vitro Diagnostic and Drug Device products will be covered throughout the course. It will be of particular interest to those seeking to introduce new Medical Devices to the market. Previous delegates who have benefited from this course include regulatory, quality, clinical and marketing managers.
Reviews
Subjects
- Market
- Benefits
- Team Training
- Medical training
- Regulations
- Medical
- Quality Training
- Marketing
- Approach
- Network
Teachers and trainers (5)
Adrian Keene
Global Medical Device Certification Manager and Head of Notified Body,
Alison Wilson
Principal Consultant, Cell Data Services, UK
Janette Benaddi
Chief Executive Officer, Medvance
Mark Charny
Managing Director, Translucency, UK
Nick Baker
Nick Baker,
Course programme
A residential rate to include 4 nights accommodation (bed & breakfast), theatre trip and buffet supper is also available when booking. Please contact our operations team if you would like this option on our Contact form.
Benefits of attending this five day course
- Understand the Procedures for Taking a Medical Device to the Market Place
- Learn what Regulations Control the Manufacture and Marketing of Devices in the EU
- Gain an Insight into Different Aspects of the Process for Obtaining the CE Mark for a Device
- Discover a Holistic Approach to Device Development and Marketing
- Participate in Workshops and Learn from Other People’s Experiences
- Understand how Other Professionals Affect the Process for Bringing a Device to Market
- Network with Participants from Organisations Similar to Your Own
Bringing a Medical Device to the market place is a complex and lengthy procedure which requires experience, knowledge and specialist skills. The contribution to a successful market placement comes from many different skilled individuals and organisations. Those contributing towards the placing of devices on the market should be aware of all the stages involved and be able to relate their responsibilities to the needs of other professionals, scientists, clinicians and regulatory and quality experts.
This comprehensive course has been designed to map the processes from device concept to marketing and show how regulatory, quality, clinical and other aspects of device development are joined into a continuous process. It will commence with a general introduction as to what devices are and how they are developed, and continue with lectures, workshops and case studies covering each process applicable to device development, marketing and eventually the post market procedures. There will be ample time for informal discussions alongside the presentations and workshops.
The Medical Device Summer School - From Concept to CE Marking