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CONDUCTING PRE AND POST MARKET MEDICAL DEVICE CLINICAL STUDIES (description)

"CONDUCTING PRE AND POST MARKET MEDICAL DEVICE CLINICAL STUDIES"

Category:Medical Education
Address:The Harrington Hall Hotel London, , United Kingdom SW7
Phone:44 1483 570099
Event dates:2/9/2006 - 2/10/2006 (This event has already taken place)
Event web site:http://www.management-forum.co.uk/html/con_semin_s
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Management Forum Ltd

Speakers/Presenters:

Topics to be Covered:

  • This course has been designed specifically for those involved in pre and post market studies within the medical device industry. The device development process can be complex, costly and can take years to complete. The collection of clinical data to demonstrate safety and performance of a device is pivotal to the development process and necessary for regulatory approval. The collection of post market data is a key aspect of continued safety and performance considerations once the device is on the market. This course will cover the full range of clinical research activities that should be applied during the collection of data for both pre and post market studies. It will provide delegates with information on the European regulations for conducting medical device studies and help them to run studies in Europe. Delegates should benefit from the advice and tips on the practicalities of conducting studies within Europe. There will be ample time for case studies and group discussion.
Contact:info@management-forum.co.uk
Organizer phone:44 1483 570099
Offering type:Conference
Specialty:Medical Education
Event frequency:Every Year
First Meeting:
Total events:
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Target audience:Any
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Host Sponsor:
Est. # of exhibitors:
Currency:Euro
Language:English
CE Credits:
Organizer URLwww.management-forum.co.uk

Description:

This course has been designed specifically for those involved in pre and post market studies within the medical device industry. The device development process can be complex, costly and can take years to complete. The collection of clinical data to demonstrate safety and performance of a device is pivotal to the development process and necessary for regulatory approval. The collection of post market data is a key aspect of continued safety and performance considerations once the device is on the market. This course will cover the full range of clinical research activities that should be applied during the collection of data for both pre and post market studies. It will provide delegates with information on the European regulations for conducting medical device studies and help them to run studies in Europe. Delegates should benefit from the advice and tips on the practicalities of conducting studies within Europe. There will be ample time for case studies and group discussion.

Schedule:

Registration Fee Details:

Other items that tuition includes:

Travel and hotel arrangements:

 
 
Contact Person:Barbara McManus / Leigh White
TitleHead of Buisness Development / Marketing Assistant
Contact Emailinfo@management-forum.co.uk
Organizer Address 148 Woodbridge Road
Organizer Address 2Guildford
Organizer CitySurrey
Organizer State/Province: (Outside US)
Organizer Zip or Postal CodeGU1 4RJ
Organizer CountryUnited Kingdom
Organizer Phone44 1483 570099
Organizer Fax44 1483 536424
Structural makeupOrganization
Event Site/VenueThe Harrington Hall Hotel, London
Event sold out?No
Multiple locations or dates?No
Statistics available for most recent event held in:NA
Average number in event attendance of:
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Number in attendance of:
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Target BoundariesLocal
Is Registration contact information the same as Organizer Contact above?Yes
Web Page
Can one register for your CE on your web site?Yes
E-mail registration:info@management-forum.co.uk
Can registration be made by snail (regular) mail?Yes
Online housing reservations: 
 
Do you have additional written or AV materials for sale?No
If so, are they available for non-attendees as well as those attending?NA
Is full tuition necessary to ensure registration?No
Will there be shuttle service available?NA

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