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

"CONDUCTING PRE AND POST MARKET MEDICAL DEVICE CLINICAL STUDIES"

Category:Clinical Chemistry
Address:The Rembrandt Hotel London, , United Kingdom SW7
Phone:+44 (0) 1483 730071
Event dates:11/2/2006 - 11/3/2006 (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 wtihin 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 willl cover the full range of clinical research activities taht 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 discussions.
Contact:info@management-forum.co.uk
Organizer phone:+44 (0) 1483 730071
Offering type:Conference
Specialty:Clinical Chemistry
Event frequency:Every Year
First Meeting:
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Est. attendance:
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 wtihin 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 willl cover the full range of clinical research activities taht 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 discussions.

Schedule:

Registration Fee Details:

Other items that tuition includes:

Travel and hotel arrangements:

 
 
Contact Person:Barbara McManus / Leigh White
TitleHead of Business Development / Marketing Assistant
Contact Emailinfo@management-forum.co.uk
Organizer Address 198-100 Maybury Road
Organizer Address 2Woking
Organizer CitySurrey
Organizer State/Province: (Outside US)
Organizer Zip or Postal CodeGU21 5JL
Organizer CountryUnited Kingdom
Organizer Phone+44 (0) 1483 730071
Organizer Fax+44(0)1483 730008
Structural makeupOrganization
Event Site/VenueThe Rembrandt 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 BoundariesInternational
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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