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FDA Medical Device Inspections - Is your company prepared?
6th December 2012 — 7th December 2012

14:14 EDT 25th May 2013 | BioPortfolio

FDA Medical Device Inspections - Is your company prepared?

BENEFITS IN ATTENDING:

  • Understand how FDA prioritises device inspection and what authority they have
  • Take away basic elements to write your FDA Inspection Policy
  • Gain practical advise on how you can be prepared for a QSIT inspection
  • Learn how the FDA prepares for an inspection
  • Know how to handle difficult situations during an inspection
  • Discuss FDA inspection trends
  • Learn the Top 10 FDA warning letter citations
  • Know how and when to responsd to form 483s warning letters

If you have any queries please contact Andrea James at andrea.james@management-forum.co.uk

Suggested Attendees

Senior Management, Regulatory Affairs, Quality Assurance, Compliance, Production, Engineering, Quality Control and Research and Development Personnel who will be involved with an FDA inspection will find this seminar essential.

Expected Number of Attendees

0-50

View Conference Website: FDA Medical Device Inspections - Is your company prepared?

Contact

Name: Leigh White
Email: info@management-forum.co.uk
Tel.: +44 (0) 1483 730071
URL: Website

Price of Attendance

£1250 + VAT

Brochure

View Event Brochure

Location

The Rembrandt Hotel
11 Thurloe Place
London
United Kingdom
SW7 2RS

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