• Webinar Jam

    Conduct webinars with up to 10 simultaneous active speakers, all being able to broadcast their respective webcam, their screen, their slide presentation.

    Learn More
  • teleseminar services

    Instant Teleseminar

    Connect to Customers from Around the World for Free!

    Learn More
  • Easy Webinar

    EasyWebinar Creates the Most Engaged and Profitable Marketing Funnels on the Planet

    Learn More
  • Your Business/Webinar Here

    Promote your webinar here.

    Buy

The 11 Must-have Documents of Software Verification and Validation

Sign up to be notified of new teleseminars daily!

Teleseminar notification signup

Description: This webinar focuses on the verification and validation planning and execution of software after basic developmental testing and de-bug. A suggested 11-element FDA model will be evaluated, implemented, with V&V documentation and test case examples.

Why Should You Attend:
Recently a major pharma company paid a $750 M fine for poor compliance, and software V&V was one of the key contributors.
Product, production / test equipment, and even the QMS are heavily software / firmware driven in today's manufacturing. A comprehensive, corporate wide plan is a necessity. Growing "cloud" issues add urgency to upgrade control. Software's complex logic pathways mandate resource-intensive V&V activities, in a resource-constrained environment.
This presentation focuses on the verification and validation planning and execution of software after basic developmental testing and de-bug. It includes COTS (commercial off-the-shelf) and growing "cloud"-based software. A suggested 11-element FDA model will be evaluated, implemented, with V&V documentation and test case examples. The focus will be on the most recent issues the FDA has had in this area, and remediation approaches. Software considered: 1) In-product, 2) As-product, 3) Production and test, and 4) QMS / 21 CFR Pt. 11. Field examples, good and bad will be addressed. Evaluation of the chief areas of FDA concerns will focus on actual and anticipated changes in emphasis based on the changing regulatory climate.
This session will help attendees understand and recognize the most common software V&V failings and their fixes. The webinar will allow attendees to develop and use a repeatable software V&V template for all software validation projects.


URL: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=703097?channel=telesemin
Date: Tuesday, September 17, 2013
Time: 2:00pm-3:00pm UTC
Duration: 1 hour
Access: Public
Category: Business*, Webinar*
Created by: Public Access
Updated: Friday, August 30, 2013 10:43am UTC
Cost ($): $299
Call In Number: +1-650-620-3915
Contact Email: referral@complianceonline.com
Contact Person: Referral
Contact Phone: +1-650-620-3915
Comments: None



img