FDA Medical Device Inspections - Is your company prepared?
6th December 2012 — 7th December 2012
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
Location
The Rembrandt Hotel
11 Thurloe Place
London
United Kingdom
SW7 2RS