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26 27 28 29 30 * CRO / VENDOR MANAGEMENT IN THE PHARMACEUTICAL INDUSTRY
 31 * THE NEW ROLE OF THE QUALIFIED PERSON UNDER THE MEDICAL DEVICES DIRECTIVES
  
MEDICAL DEVICES
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FDA APPROVAL PROCESS
FOR MEDICAL DEVICES

Includes all the current FDA Guidelines

Conference Date: 26-27 Nov 2012
Conference Ref: N11-8012
Fee: £1250 + VAT
Venue: The Rembrandt Hotel, London

Special discounted rate available if booked together with 'FDA Adverse Event Reporting' meeting on 28 & 29 November (£2,100 + VAT)

UPON COMPLETION OF THIS SEMINAR, PARTICIPANTS WILL:

  • Understand the FDA medical deveice approval system
  • Knew what is required for an Investigational Device Exemption (IDE)
  • Learn the contents of a Post-Market Approval (PMA)
  • Discover what to include in an annual report

If you have any queries please click here to contact Andrea James

 

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