In-Vitro Diagnostics Directive (IVDD)
12th March 2013 — 13th March 2013

In-Vitro Diagnostics Directive (IVDD)

INTRODUCTION

This seminar will clarify the requirements applicable for IVDs and will look at the future proposed changes to the Directive and the implications for industry. It will also highlight the important issues regarding supplier control and validation. Practical workshop exercises throughout the day will help consolidate the information provided.

WHO SHOULD ATTEND

• Regulatory Affairs Personnel
• Quality Assurance Professionals
• Those responsible for Original Equipment Manufacturer (OEM) / subcontractor control of IVD’s

Benefits in Attending:

• Understand the IVD Directive
• Prepare for the Revision of the IVD Directive
• Take Away Techniques on Conformity with the Essential Requirements
• Gain Essential Information on Supplier Control
• Apply the Principles in Practical Exercises and Workgroup Sessions

With
Ann Goodall, IVD Product Specialist, BSi Healthcare

Suggested Attendees

• Regulatory Affairs Personnel • Quality Assurance Professionals • Those responsible for OriginalEquipment Manufacturer (OEM) / Subcontractor control of IVD's

Expected Number of Attendees

0-50

View Conference Website: In-Vitro Diagnostics Directive (IVDD)

Price of Attendance

£1260 + VAT

Brochure

View Event Brochure

Location

Harrington Hall Hotel
5-25 Harrington Gardens
London
United Kingdom
SW7 4JW