Book Online Tickets for Drafting a Software Verification and Val, Palo Alto.  
A tougher U.S. FDA expects a company to maintain certain documents in equipment, process and product software V&V. These documentation requirements can assist in a 21 CFR Part 11 CGMP records / signature V&V as well. This training prog

Drafting a Software Verification and Validation Report Package and Protocol - The 11 Must-have Documents

 

  • One Dial-in One Attendee

    Last Date: 04-12-2018

    USD 199
  • Group-Max 10 Attendees or Location

    Last Date: 04-12-2018

    USD 529
  • 1 Person - Unlimited viewing for 6 Months

    Last Date: 04-12-2018

    USD 249
  • One CDorUSB is for usage in one location only

    Last Date: 04-12-2018

    USD 349
  • LIVE and RECORDED VERSION

    Last Date: 04-12-2018

    USD 349
  • LIVE and TRAINING CD or USB

    Last Date: 04-12-2018

    USD 449

Invite friends

Contact Us

Page Views :

About The Event

 

A tougher U.S. FDA expects a company to maintain certain documents in equipment, process and product software V&V. These documentation requirements can assist in a 21 CFR Part 11 CGMP records / signature V&V as well. This training program will provide valuable assistance to all regulated companies in evaluating their existing or anticipated software V&V activities and documentation requirements, especially in light of the changes in the FDA's stance vis a vis industry compliance, past problems, and the growing cloud environment. It 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.