MEDICAL DEVICES 2011 - Practical Project Management for FDA-Regulated Companies - Webinar By ComplianceOnline

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Category Medical Devices,conference,event,Webinar

Deadline: March 08, 2011 | Date: March 08, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2011-02-02 18:21:48 (GMT+9)

Call For Papers - CFP

The FDA expects companies to manage projects formally -- to include regulatory requirements, design and/or change control, with consideration of all applicable standards. The EU MDD and their notified bodies are no different.

This Project Management for FDA-Regulated Companies webinar will provide valuable guidance to regulated companies in development and implementation of Project Management Planning and Techniques for new product development, regulatory compliance audit responses, proof of "progress against plan", and other activities requiring a planned documented rationale. We will discuss one very simple approach using common Excel- or Word-type PC applications programs that can be used immediately. Three of the most common tools will be discussed. Regular use of a few simple but powerful tools will be showcased which will virtually eliminate "fire fighting" in a new project.

Areas Covered in the Seminar:

Meet key requirements of the CGMPs/ISO with formal project mgmt.

Why formal Project Management.

The Three Most Common Tools - Gantt, CPM, PERT.

How to Compile - Simple Spreadsheet Techniques.

Work breakdown Structure, Milestones, Tasks.

Effectiveness -- Determining and Monitoring.

A Suggested Template.

One Major, But Often Neglected, Use.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.