TUESDAY MARCH-11-2014

01:00 PM | 02:00 PM EST DURATION: 60 MINUTES

Live webinar on "How to Develop a Master Validation Plan"

Description of the topic

Every medical device company (OEM) must meet certain standards for validation of its transfer plans, facilities,
clean rooms and processes. These standards apply for OEMs and suppliers to OEMs. This webinar on How to
Develop a Master Validation Plan (also known as Validation Master Plan) will provide a step-by-step procedure
for all medical device companies and their suppliers that are in need of developing a plan for
product/equipment transfer, facilities, processes or to develop a company standard.

Why should you attend :

Many medical companies have never had a Master Validation Plan for their facilities, processes or suppliers.
This is an important standard to have when being audited to show on a big picture compliance to FDA and
foreign standards. This webinar defines the step-by-step procedure for all medical device companies and their
suppliers that are in need of developing a plan for product/equipment transfer, facility, processes or to develop
a company standard.
Areas Covered in the Session:
Master Validation Plan content
Revision history
Background
Objective
Purpose
Scope
Project approach
Key activities
Project organization
Communication plan
Quality Assurance
Facility approach
Validation approach.

Live
One Dial In - One
$189Attendee
One Dial In Unlimited
attendance (To be
arranged in a
$249Conference
room/Meeting
room. Note : Only
One Dial In
Allowed)

Combo
Combo 1 (One Dial
In - Unlimited
$329attendance + On
Demand Recorded
Session)
Combo 2 (One Dial
In - Unlimited
$349
attendance +
Training CD)

Recorded
On Demand ( 90
Days of online
$289Streaming access
available after the
live session )
Play Back Unlimited Views
( Recorded file
$319
available for
download after the
live session )
Get Training CD
$359

Multiple
Location
$109 Multiple location
9
- Up to 5 Dial in
$499 allowed

Schedule
Budget and more

This webinar will provide valuable assistance and give a guide lines and a
procedure for regulated companies that need to develop a Master
Validation Plan for facilities, new and mature products and processes.
Who will benefit:
The employees who will benefit include:
OEM Senior management
Supplier Senior management
Managers and directors
Managers setting up new facilities and product lines
Plant and facility managers
End-users responsible for design control and product development
R&D and product development
Project managers
Facility and clean room designers
Process engineers and managers
Validation engineers
Quality management and engineers
Auditors
Suppliers to medical OEMs
Consultants

For any assistance contact us at support@compliance2go.com or call us

at 877.782.4696 Or Visit us:-

pid=CP2014-278

https://www.compliance2go.com/product/?