Seminar on Validation and 21 CFR 11 Compliance of Computer Systems | September 3, 2015 9:00 AM - September 4, 2015 6:00 PM | Automation.com

Seminar on Validation and 21 CFR 11 Compliance of Computer Systems

Event Summary

DATE:
September 3, 2015 - September 4, 2015
LOCATION:
Washington, DC 20003
COUNTRY:
United States
START DATE/TIME:
September 3, 2015 9:00 AM
END DATE/TIME:
September 4, 2015 6:00 PM
EVENT TYPE:
Seminar
HOST:
GlobalCompliancepanel
PHONE:
18004479407
EMAIL:
[email protected]
WEBSITE:
Click here to Visit

Description

The Problem:
Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and / or international regulations or business continuity requirements. In addition, the FDA has stepped up 21 CFR 11 inspections that include CSV.
This course will build on the Validation and 21 CFR 11 Compliance Basic Course, to give hands on experience on executing on the computer systems validation of a system, and to discuss related activities such as Validation Master Plan, Infrastructure Qualification, Project Management for Validation and Validation of Test Tools
The attendees must have attended the Basic Validation & 21 CFR 11 Compliance. This is a very hands-on class and the attendees will be expected to use templates provided in the class to create the complete package for the validation of a system
The Seminar:
This Hands-On course will provide the attendees with more detailed experience on validation / 21 CFR 11 compliance of a computer system, as well as details for activities associated with computer systems validation as follows:
1. Validation Master Plan
2. Complete Validation for a System
3. Excel Spreadsheet Validation
4. Change Control
5. SOPs
6. Test Tools Validation
7. Project Management for Validation
Course Description:
Day 1 – Agenda
Lecture 1: Introduction / Background
• Introductions / Participants' Understanding
• Participants' Objectives for the Course (Please come prepared to discuss)
Lecture 2: Requirements at a High Level
• Types of Requirements
• Difference between User Requirements & Functional Requirements
Lecture 3: Detailed Requirements Study
• Gathering Requirements
• Entity Relationship Diagram
• Process Decomposition
• Risk Assessment for Requirements
• Exercise on how to create Requirements
Lecture 4: Design
• Design Specifications
• Software Configuration and Build
• Exercise on how to create Design Specifications
Day 2 – Agenda
Lecture 5: CSV Detailed Study (Cont'd)
• Traceability Matrix
• Verification and Testing
• Exercise Creating Validation Scripts
• Exercise Creating Traceability Matrix
Lecture 6: Other Documents
• Validation Plan
• Test Protocols
• Validation Report
• Validation Registry
Lecture 7: Special Topics
• Project Management for CSV
• Infrastructure for CSV
• Selecting software for 21 CFR 11 Compliance
• Test Tools for CSV
Lecture 8: Change Control & Business Continuity
• Change Control
• Implementing Business Continuity for CSV
Who Should Attend?
• VP of IT
• Director of IT
• Quality Managers
• Project Managers (for CSV / IT)
• Validation Specialists
• Database Administrators
• System Administrators
• Directors / Senior Directors of Discovery
• Directors / Senior Directors of Development
• Directors / Senior Directors of Commercialization
• Document Managers
• Training Managers
Industries:
• Pharmaceuticals
• Biotech
• Medical Device
• Radiological Health
• Blood Products
• Companion Animals
• Food
• Cosmetics
• Tobacco
• Academia
Instructor Profile:
Angela Bazigos is the CEO of Touchstone Technologies Silicon Valley, Inc. "Your Passport to Compliance". She has 30 years of experience in the Life sciences industry spanning Project Management, Quality Assurance and Regulatory Affairs and has a patent aimed at speeding up Software Compliance.
Ms Bazigos is a member of the SQA CVIC (Society of Quality Assurance Computer Validation Initiative Committee), ASQ, DIA and RAPS and consults to investment groups on Life sciences investments as well as Pharma / Biotech / Medical Device companies on compliance matters, including strategy, submissions, quality
Date, Time and Venue:
Location: Washington DC
Date: September 3rd and 4th, 2015
Time: 9am to 6pm
Venue/Hotel: WILL BE ANNOUNCED SOON

Ticket Price and Discount:
Price: $1,695.00 (Seminar for One Delegate)
Register now and save $200. (Early Bird)
Until July 31, Early Bird Price: $1,695.00
From August 01 to September 01, Regular Price: $1,895.00

Contact Information:
NetZealous LLC, DBA GlobalCompliancePanel
161 Mission Falls Lane,
Suite 216, Fremont, CA 94539, USA
USA Phone: 800-447-9407
Fax: 302-288-6884
[email protected]
http://www.globalcompliancepanel.com
Event Registration Link - http://bit.ly/1IV37Sf

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