MEDICAL DEVICES 2011 - Change Control Systems for Medical Devices Current Best Practices for FDA-Compliant Systems - Medical Devices webinar By ComplianceOnline

Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701785?channel=ourglocal | Edit Freely

Category Medical Devices,conference,event,Webinar

Deadline: January 18, 2011 | Date: January 18, 2011

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

Updated: 2010-12-03 18:09:33 (GMT+9)

Call For Papers - CFP

It is well known that document change control is a critical requirement for FDA-regulated companies. However, this can be a time- and paper-consuming process, in which even the simplest of changes requires an inordinate amount of time spent in the preparation, submission, distribution, and implementation of change requests, document modifications, document review meetings, document approvals, and document placement. The best document change control systems are those that are fast and effective.

This presentation will review the QSR requirements for document change control, and provide a streamlined process - Many companies can spend MUCH LESS preparing MANY FEWER documents, and still be in compliance with the regulations; is yours one of these?