ComplianceOnline

Register

Toll Free: +1-888-717-2436


Management Responsibility for Integrating Medical Device Design
By
Date:


Abstract:

How can various departments work together to ensure medical device design projects are executed efficiently and successfully? This responsibilitiy lies with the management - but what are the best practices that can be followed?

Dev Raheja, a renowned medical device quality expert, explains all in this article.

Click here for Detail Description
Bookmark and Share
left curve right curve

Your Shopping Cart

Refresh
Contains 0 items
Total: $0.00
Cart Image
left curve right curve

Compliance Trainings
Pregnancy in the Workplace: Strategies to Protect Your Organization from Pregnancy Discrimination Claims
On Demand Access Anytime
How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial
On Demand Access Anytime
DMR & DHR - What Is Really Required
On Demand Access Anytime
more...
Contributing Authors/ Experts
Michael Anisfeld, Senior Consultant, Globepharm Consulting Inc.
Sonia Gourary, Senior Compliance Consultant, Quality and Compliance Partners
R. Wayne Frost, President, Frost Biopharmaceutical Consulting
Compliance Standards
Evidence Product Checklist For Standard IEC 62304:2006 "Medical Device Software - Software Life Cycle Processes"
Price: $299
(New) Template Kit for Software Engineers
Price: $598
Evidence Product Checklist For Standard ISO/IEC 20000-1:2011 “Information Technology –Service Management –Part 1: Service Management System Requirements”
Price: $299
Quality Kit
Price: $748
More Standards...